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34034-87-2

34034-87-2 Structure

34034-87-2 Structure
IdentificationBack Directory
[Name]

2-CHLORO-3-OXO-SUCCINIC ACID DIETHYL ESTER
[CAS]

34034-87-2
[Synonyms]

Diethyl Chlorooxalacetate
DiethylChlorooxalacetate>
DIETHYL 2-CHLORO-3-OXOSUCCINATE
diethyl 2-chloro-3-oxobutanedioate
Chlorooxalacetic Acid Diethyl Ester
Diethyl 2-chloro-3-oxobutane-1,4-dioate
2-CHLORO-3-OXO-SUCCINIC ACID DIETHYL ESTER
Diethyl 2-chlorooxalacetate, technical, 90%
2-Chloro-3-oxo butanedioic acid 1,4-diethyl ester
Butanedioic acid, 2-chloro-3-oxo-, 1,4-diethyl ester
[EINECS(EC#)]

200-589-5
[Molecular Formula]

C8H11ClO5
[MDL Number]

MFCD04114359
[MOL File]

34034-87-2.mol
[Molecular Weight]

222.62
Chemical PropertiesBack Directory
[Boiling point ]

130 °C / 9mmHg
[density ]

1.23
[refractive index ]

1.4480
[Fp ]

108℃
[storage temp. ]

0-10°C
[form ]

clear liquid
[pka]

5.24±0.46(Predicted)
[color ]

White to Yellow to Green
Safety DataBack Directory
[Hazard Codes ]

Xi
[Hazard Note ]

Irritant
[HS Code ]

2918300090
Spectrum DetailBack Directory
[Spectrum Detail]

2-CHLORO-3-OXO-SUCCINIC ACID DIETHYL ESTER(34034-87-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethyl chloroacetate

105-39-5

Diethyl oxalate

95-92-1

2-CHLORO-3-OXO-SUCCINIC ACID DIETHYL ESTER

34034-87-2

NaOtBu (96.1 g, 1.0 mol) was dissolved in THF (1 L) and the solution was cooled to 0°C. A mixture of ethyl chloroacetate (107 mL, 1.0 mol) and diethyl oxalate (136 mL, 1.0 mol) was added slowly and dropwise at this temperature under vigorous mechanical stirring. After the reaction mixture was stirred overnight at room temperature, an aqueous HCl solution (90 mL of concentrated hydrochloric acid mixed with 400 mL of water) was added. The resulting solution was extracted with CH2Cl2 (3 x 200 mL). The organic layers were combined, dried with anhydrous Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by reduced pressure distillation (boiling point range 110-140°C, pressure 10 torr). The product diethyl 2-chloro-3-oxosuccinate was obtained 157.6 g in 71% yield.1H NMR (CDCl3, 400 MHz) δ= 1.31 (t, J = 7.2Hz, 3H), 1.39 (t, J = 7.2Hz, 3H), 4.31 (q, J = 7.2Hz, 2H), 4.39 (q, J = 7.2Hz, 2H), 4.39 (q, J = 7.2Hz, 2H) 5.46 (s, 1H).

[References]

[1] European Journal of Medicinal Chemistry, 2018, vol. 154, p. 367 - 391
[2] Patent: CN104177296, 2017, B. Location in patent: Paragraph 0043; 0044; 0045
[3] Macromolecules, 2011, vol. 44, # 23, p. 9146 - 9154
[4] Chemische Berichte, 1910, vol. 43, p. 3529
[5] Bulletin des Societes Chimiques Belges, 1975, vol. 84, p. 341 - 360
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