Synthesis of Glyoxylic Acid by Glyoxal Oxidation in the Presence of Hydrohalic Acids

A procedure was developed for preparing glyoxylic acid by glyoxal oxidation with nitric acid in the presence of hydrohalic acids with selective isolation of glyoxylic acid from the reaction mixture in the form of magnesium and calcium salts. Specific features of the synthesis of glyoxylic acid were...

Full description

Saved in:
Bibliographic Details
Published in:Russian journal of applied chemistry Vol. 93; no. 10; pp. 1571 - 1577
Main Authors: Pozdniakov, M. A., Zhuk, I. V., Salikov, A. S., Botvin, V. V., Filimoshkin, A. G.
Format: Journal Article
Language:English
Published: Moscow Pleiades Publishing 01-10-2020
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract A procedure was developed for preparing glyoxylic acid by glyoxal oxidation with nitric acid in the presence of hydrohalic acids with selective isolation of glyoxylic acid from the reaction mixture in the form of magnesium and calcium salts. Specific features of the synthesis of glyoxylic acid were demonstrated, and optimum conditions for each step of the process were determined. The highest yield of glyoxylic acid was obtained in oxidation of glyoxal with an HNO 3 : HCl mixture. Oxidation in the presence of HF and HBr is characterized by lower yields because of low dissociation constant of HF and side redox reactions with HBr. Dilute solutions of glyoxylic acid were obtained by an exchange reaction of its calcium salt with a hydrofluoric acid solution at room temperature. An increase in the reaction temperature leads to an increase in the content of glycolic and oxalic acids formed by disproportionation of glyoxylic acid in the initial step of the exchange reaction.
AbstractList A procedure was developed for preparing glyoxylic acid by glyoxal oxidation with nitric acid in the presence of hydrohalic acids with selective isolation of glyoxylic acid from the reaction mixture in the form of magnesium and calcium salts. Specific features of the synthesis of glyoxylic acid were demonstrated, and optimum conditions for each step of the process were determined. The highest yield of glyoxylic acid was obtained in oxidation of glyoxal with an HNO 3 : HCl mixture. Oxidation in the presence of HF and HBr is characterized by lower yields because of low dissociation constant of HF and side redox reactions with HBr. Dilute solutions of glyoxylic acid were obtained by an exchange reaction of its calcium salt with a hydrofluoric acid solution at room temperature. An increase in the reaction temperature leads to an increase in the content of glycolic and oxalic acids formed by disproportionation of glyoxylic acid in the initial step of the exchange reaction.
Author Pozdniakov, M. A.
Botvin, V. V.
Zhuk, I. V.
Filimoshkin, A. G.
Salikov, A. S.
Author_xml – sequence: 1
  givenname: M. A.
  surname: Pozdniakov
  fullname: Pozdniakov, M. A.
  organization: National Research Tomsk State University
– sequence: 2
  givenname: I. V.
  surname: Zhuk
  fullname: Zhuk, I. V.
  organization: National Research Tomsk State University
– sequence: 3
  givenname: A. S.
  surname: Salikov
  fullname: Salikov, A. S.
  organization: National Research Tomsk State University
– sequence: 4
  givenname: V. V.
  surname: Botvin
  fullname: Botvin, V. V.
  email: v.v.botvin@gmail.com
  organization: National Research Tomsk State University
– sequence: 5
  givenname: A. G.
  surname: Filimoshkin
  fullname: Filimoshkin, A. G.
  organization: National Research Tomsk State University
BookMark eNp1kFFLwzAUhYNMcJu--5g_UL25bdP2cQzdhMGEzeeSponLqIkkFdZ_b0r1RfDpXu453-VwFmRmnVWE3DN4YCzNHg8MCsiwQAQGDPGKzBmHMkmx4rO4RzUZ5RuyCOEMABXn5ZwcD4PtTyqYQJ2mm25wl6Ezkq6kaWkzTBfR0f3FtKI3zlJjaQToq1dBWalGbDu03p3ELxduybUWXVB3P3NJ3p6fjuttsttvXtarXSJTxD7RnGdYCa6LtsWWN1qmUjYF6KJSJWSl0CzGBI4Scp1zzEHzNCuxyEFik5XpksD0V3oXgle6_vTmQ_ihZlCPrdR_W4kIm5AQrfZd-frsvryNKf9nvgH-nmSB
CitedBy_id crossref_primary_10_1177_00037028221123091
crossref_primary_10_1002_slct_202201140
crossref_primary_10_1016_j_fuel_2024_132198
Cites_doi 10.1002/14356007.a12_495
10.1080/01496395.2016.1269129
10.1021/j100344a021
10.1016/B978-0-12-697252-8.50009-1
10.1007/s11172-019-2442-2 
10.1007/s11172-019-24881 
ContentType Journal Article
Copyright Pleiades Publishing, Ltd. 2020
Copyright_xml – notice: Pleiades Publishing, Ltd. 2020
DBID AAYXX
CITATION
DOI 10.1134/S107042722010122
DatabaseName CrossRef
DatabaseTitle CrossRef
DatabaseTitleList
DeliveryMethod fulltext_linktorsrc
Discipline Engineering
Chemistry
EISSN 1608-3296
EndPage 1577
ExternalDocumentID 10_1134_S107042722010122
GroupedDBID -58
-5G
-BR
-EM
-Y2
-~C
-~X
.86
.VR
06C
06D
0R~
0VY
123
1N0
29P
2J2
2JN
2JY
2KG
2KM
2LR
2P1
2VQ
2~H
30V
4.4
408
409
40D
40E
5VS
642
67Z
6NX
8TC
8UJ
95-
95.
95~
96X
AAAVM
AABHQ
AAFGU
AAHNG
AAIAL
AAJKR
AANZL
AAPBV
AARHV
AARTL
AATNV
AATVU
AAUYE
AAWCG
AAYFA
AAYIU
AAYQN
AAYTO
ABBBX
ABBXA
ABDZT
ABECU
ABEFU
ABFGW
ABFTV
ABHLI
ABHQN
ABJNI
ABJOX
ABKAS
ABKCH
ABKTR
ABMNI
ABMQK
ABNWP
ABPTK
ABQBU
ABSXP
ABTEG
ABTHY
ABTKH
ABTMW
ABULA
ABWNU
ABXPI
ACBMV
ACBRV
ACBXY
ACBYP
ACGFS
ACHSB
ACHXU
ACIGE
ACIPQ
ACIWK
ACKNC
ACMDZ
ACMLO
ACOKC
ACOMO
ACREN
ACSNA
ACTTH
ACVWB
ACWMK
ADHHG
ADHIR
ADINQ
ADKNI
ADKPE
ADMDM
ADOXG
ADRFC
ADTPH
ADURQ
ADYFF
ADYOE
ADZKW
AEBTG
AEFTE
AEGAL
AEGNC
AEJHL
AEJRE
AEKMD
AENEX
AEOHA
AEPYU
AESTI
AETLH
AEVLU
AEVTX
AEXYK
AFGCZ
AFLOW
AFNRJ
AFQWF
AFWTZ
AFYQB
AFZKB
AGAYW
AGDGC
AGGBP
AGJBK
AGMZJ
AGQMX
AGWIL
AGWZB
AGYKE
AHAVH
AHBYD
AHSBF
AHYZX
AIAKS
AIIXL
AILAN
AIMYW
AITGF
AJBLW
AJDOV
AJRNO
AKQUC
ALMA_UNASSIGNED_HOLDINGS
ALWAN
AMKLP
AMTXH
AMXSW
AMYLF
AMYQR
AOCGG
ARMRJ
ASPBG
AVWKF
AXYYD
AZFZN
B-.
BA0
BDATZ
BGNMA
CAG
COF
CS3
CSCUP
DDRTE
DL5
DNIVK
DPUIP
DU5
EBLON
EBS
EIOEI
EJD
ESBYG
FEDTE
FERAY
FFXSO
FIGPU
FINBP
FNLPD
FRRFC
FSGXE
FWDCC
G-Y
G-Z
GGCAI
GGRSB
GJIRD
GNWQR
GQ6
GQ7
GQ8
GXS
HF~
HG6
HLICF
HMJXF
HQYDN
HRMNR
HVGLF
HZ~
IHE
IJ-
IKXTQ
IWAJR
IXC
IXD
IXE
IZIGR
IZQ
I~X
I~Z
J-C
JBSCW
JCJTX
JZLTJ
KDC
KOV
LAK
LLZTM
M4Y
MA-
N2Q
NB0
NPVJJ
NQJWS
NU0
O9-
O93
O9J
OAM
OVD
P9N
PF0
PT4
QOR
QOS
R89
R9I
RIG
RNI
RNS
ROL
RPX
RSV
RZC
RZE
S16
S1Z
S27
S3B
SAP
SCM
SDH
SHX
SISQX
SJYHP
SNE
SNPRN
SNX
SOHCF
SOJ
SPISZ
SQXTU
SRMVM
SSLCW
STPWE
SZN
T13
TEORI
TSG
TSK
TSV
TUC
U2A
UG4
UNUBA
UOJIU
UTJUX
UZXMN
VC2
VFIZW
W23
W48
WJK
WK8
XU3
YLTOR
Z5O
Z7R
Z7S
Z7U
Z7V
Z7W
Z7X
Z7Y
Z7Z
Z83
Z88
ZMTXR
~A9
AACDK
AAJBT
AASML
AAYXX
AAYZH
ABAKF
ACAOD
ACDTI
ACZOJ
AEFQL
AEMSY
AFBBN
AGRTI
AIGIU
CITATION
H13
ID FETCH-LOGICAL-c322t-f66429a6f7dd2d6bfc3ccb70f79e8048af1009062c05f56250f63482750c2b483
IEDL.DBID AEJHL
ISSN 1070-4272
IngestDate Fri Nov 22 00:22:02 EST 2024
Sat Dec 16 11:59:34 EST 2023
IsPeerReviewed true
IsScholarly true
Issue 10
Keywords alkaline earth metal salts
glyoxylic acid
oxalic acid
glyoxal oxidation
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c322t-f66429a6f7dd2d6bfc3ccb70f79e8048af1009062c05f56250f63482750c2b483
PageCount 7
ParticipantIDs crossref_primary_10_1134_S107042722010122
springer_journals_10_1134_S107042722010122
PublicationCentury 2000
PublicationDate 2020-10-01
PublicationDateYYYYMMDD 2020-10-01
PublicationDate_xml – month: 10
  year: 2020
  text: 2020-10-01
  day: 01
PublicationDecade 2020
PublicationPlace Moscow
PublicationPlace_xml – name: Moscow
PublicationTitle Russian journal of applied chemistry
PublicationTitleAbbrev Russ J Appl Chem
PublicationYear 2020
Publisher Pleiades Publishing
Publisher_xml – name: Pleiades Publishing
References OgataY.Org. Chem. Part C197838129510.1016/B978-0-12-697252-8.50009-1
SrinivasakannanC.VasanthakumarR.IyappanK.RaoP.G.Chem. Biochem. Eng. Q.2002161251:CAS:528:DC%2BD38XptF2qtb0%3D
Patent US 8426632 B2, Publ. 2013.
PozdniakovM.RubtsovK.BotvinV.SorvanovA.KnyazevA.FilimoshkinA.Sep. Sci. Technol.2017528761:CAS:528:DC%2BC2sXitVKju7s%3D10.1080/01496395.2016.1269129
PozdniakovM.A.SalikovA.S.BotvinV.V.PoleshchukO.K.FilimoshkinA.G.Russ. Chem. Bull.2019688021:CAS:528:DC%2BC1MXhtVajur%2FN10.1007/s11172-019-24881
PozdniakovM.A.ZhukI.V.LyapunovaM.V.SalikovA.S.BotvinV.V.FilimoshkinA.G.Russ. Chem. Bull.2019684721:CAS:528:DC%2BC1MXos1Sqsrk%3D10.1007/s11172-019-2442-2
MattiodaG.ChristidisY.Ullmann’s Encyclopedia of Industrial Chemistry200217891:CAS:528:DC%2BB3cXjslGmtrs%3D10.1002/14356007.a12_495
Patent US 8754255 B2, Publ. 2008.
LengyelI.NagyI.BazsaG.J. Phys. Chem.19899328011:CAS:528:DyaL1MXhsVaiu78%3D10.1021/j100344a021
Patent RU 2541790, Publ. 2015.
M.A. Pozdniakov (3165_CR7) 2019; 68
C. Srinivasakannan (3165_CR9) 2002; 16
Y. Ogata (3165_CR6) 1978; 381
I. Lengyel (3165_CR8) 1989; 93
3165_CR10
M. Pozdniakov (3165_CR4) 2017; 52
G. Mattioda (3165_CR3) 2002; 17
3165_CR2
3165_CR5
M.A. Pozdniakov (3165_CR1) 2019; 68
References_xml – volume: 17
  start-page: 89
  year: 2002
  ident: 3165_CR3
  publication-title: Ullmann’s Encyclopedia of Industrial Chemistry
  doi: 10.1002/14356007.a12_495
  contributor:
    fullname: G. Mattioda
– volume: 16
  start-page: 125
  year: 2002
  ident: 3165_CR9
  publication-title: Chem. Biochem. Eng. Q.
  contributor:
    fullname: C. Srinivasakannan
– volume: 52
  start-page: 876
  year: 2017
  ident: 3165_CR4
  publication-title: Sep. Sci. Technol.
  doi: 10.1080/01496395.2016.1269129
  contributor:
    fullname: M. Pozdniakov
– volume: 93
  start-page: 2801
  year: 1989
  ident: 3165_CR8
  publication-title: J. Phys. Chem.
  doi: 10.1021/j100344a021
  contributor:
    fullname: I. Lengyel
– ident: 3165_CR2
– volume: 381
  start-page: 295
  year: 1978
  ident: 3165_CR6
  publication-title: Org. Chem. Part C
  doi: 10.1016/B978-0-12-697252-8.50009-1
  contributor:
    fullname: Y. Ogata
– ident: 3165_CR10
– volume: 68
  start-page: 472
  year: 2019
  ident: 3165_CR1
  publication-title: Russ. Chem. Bull.
  doi: 10.1007/s11172-019-2442-2 
  contributor:
    fullname: M.A. Pozdniakov
– volume: 68
  start-page: 802
  year: 2019
  ident: 3165_CR7
  publication-title: Russ. Chem. Bull.
  doi: 10.1007/s11172-019-24881 
  contributor:
    fullname: M.A. Pozdniakov
– ident: 3165_CR5
SSID ssj0009668
Score 2.255917
Snippet A procedure was developed for preparing glyoxylic acid by glyoxal oxidation with nitric acid in the presence of hydrohalic acids with selective isolation of...
SourceID crossref
springer
SourceType Aggregation Database
Publisher
StartPage 1571
SubjectTerms Chemistry
Chemistry and Materials Science
Chemistry/Food Science
Industrial Chemistry/Chemical Engineering
Organic Synthesis and Industrial Organic Chemistry
Title Synthesis of Glyoxylic Acid by Glyoxal Oxidation in the Presence of Hydrohalic Acids
URI https://link.springer.com/article/10.1134/S107042722010122
Volume 93
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NS8MwFA-6HdSDH1NxfpGDF4Vom3ZJexxzWxVRYRO8lTQfWBytrBus_71JP9SJHvRUCO-F8pqX9359ye8BcIYF8x3P4khGRAMUxxeIuVIgzEnEhdAomxugGIzo_bN33Tc0OfbHr4vk9bKuSBYbddl2xL0aaZxi-kJgU761sd51mzrydPTSbnb7t8HdJ9Muqe6_UQsZ-bo2-cMcy7FouRBaxJfB1j_ebBtsVskk7JZffwesyKQF1np1D7cW2PhCN7gLxqM80fleFmcwVXA4ydNFPok57PJYwCgvR_R8D4u47LQE4wRqBfhY3FHi0qgFuZimL6zWy_bA06A_7gWo6qqAuHbeGVJEQw6fEUWFwIJEijucR9RS1Jee9membG1Ei2BudZSBR5YihgFHpxYcR67n7INGkibyAEDhYcbNKPEdl0jFuM90umkrKimhtNMG57V9w7eSPCMsQIfjht-t1gYXtXXDyo2yX4UP_yJ8BNaxAcnFCbxj0JhN5_IErGZiflqtHfO8GQ8H72jHvDk
link.rule.ids 315,782,786,27933,27934,41073,42142,48344,48347,49649,49652,52153
linkProvider Springer Nature
linkToHtml http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LS8NAEB60PVQPPqpife7Bi0Iw3aS7ybFU2xRrFVrBW0j2gYGSSNNC8-_dzQOt6EGvy8yyzO7szsfszAdwhXngWo7JDBESBVAslxuBLbiBGQkZ5wplMw0UvQkdvzp397pNDq5qYfLf7lVKMr-pC94R-3aigIomhsA6f9vG6tqt2y6x1Umud4fTQf-z1S4pC-CoaWj5Kjn5wxzrj9F6JjR_YPq7_1naHuyU4STqFvu_DxsibkKjV7G4NWH7S8PBA5hOslhFfGmUokSiwSxLVtksYqjLIo7CrBhR8z2tooJrCUUxUgroOa9SYkKreRmfJ29BpZcewkv_ftrzjJJXwWDKfReGJAp0uAGRlHPMSSiZxVhITUld4SiPDmRbWdEkmJkdqQGSKYnugaOCC4ZD27GOoBYnsTgGxB0cMD1KXMsmQgbMDVTA2ZZUUEJppwXXlYH996J9hp_DDsv2v1utBTeVdf3SkdJfhU_-InwJDW_6OPJHw_HDKWxhDZnz_3hnUFvMl-IcNlO-vCgP0gfoZb6b
linkToPdf http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1LS8NAEF60BR8HH1WxPvfgRSE03aS7yUUofRi11EIreAubfWCgJKVpofn37uaBVvQgXoeZJQwz2fmYnW8AuEGcupZjMkMEWAEUy-UGtQU3EMMB41yhbKaBojcmwzen29M0OfflLEz22r1sSeYzDZqlKVo0ZlwWO0jsxliBFr0kAulebhOpX3DVViIV59V278kbfNLu4mIYjpiG1i8blT-csX4xrXdFs8umv__fzzwAe0WZCdt5XByCDRHVwHan3O5WA7tfiAiPwGScRqoSTMIExhI-TNN4lU5DBtss5DBIc4k672UV5juYYBhBZQBH2fQSE9rMS_k8fqelXXIMXvu9Scczin0LBlNpvTAkVmDEpVgSzhHHgWQWYwExJXGFozKdyqbyqIkRM1tSAydTYs2No4oOhgLbsU5AJYojcQogdxBlWopdy8ZCUuZSVYg2JREEE9Kqg9vS2f4sp9XwMzhi2f53r9XBXelpv0iw5Ffls78oX4OtUbfvDx6Hz-dgB2kknT3TuwCVxXwpLsFmwpdXRUx9AOJDx14
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Synthesis+of+Glyoxylic+Acid+by+Glyoxal+Oxidation+in+the+Presence+of+Hydrohalic+Acids&rft.jtitle=Russian+journal+of+applied+chemistry&rft.au=Pozdniakov%2C+M.+A.&rft.au=Zhuk%2C+I.+V.&rft.au=Salikov%2C+A.+S.&rft.au=Botvin%2C+V.+V.&rft.date=2020-10-01&rft.pub=Pleiades+Publishing&rft.issn=1070-4272&rft.eissn=1608-3296&rft.volume=93&rft.issue=10&rft.spage=1571&rft.epage=1577&rft_id=info:doi/10.1134%2FS107042722010122&rft.externalDocID=10_1134_S107042722010122
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1070-4272&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1070-4272&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1070-4272&client=summon