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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902799Generated: November 1, 2026

Oxalyl chloride → 2-Methoxyimino-3-oxo-butanoyl chloride

https://huagongshe.com/reaction/1902799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-Methoxyimino-3-oxobutyric acidHCID 54183495—
CatalystDimethylformamideHCID 6228—
SolventDiethyl EtherHCID 3283—
Product2-Methoxyimino-3-oxo-butanoyl chlorideHCID 54108040—

Reaction Conditions

Temperature20 °C

Reaction Steps

Dimethylformamide (2 drops) is added to a solution, at 20° C., of 2-methoxyimino-3-oxo-butyric acid, syn isomer (4.08 g) in diethyl ether (50 cc), after which oxalyl chloride (2 cc) dissolved in diethyl ether (5 cc) is added dropwise in the course of 15 minutes. The mixture is stirred for 1 hour at 20° C., dimethylformamide (1 drop) is added again and the reaction is continued for 15 minutes. The mixture is concentrated to dryness at 20° C. under 20 mm Hg (2.7 kPa) and the residue is taken up in petroleum ether (2×30 cc), the solvent being evaporated each time at 20° C. under 20 mm Hg (2.7 kPa). The 2-methoxyimino-3-oxo-butanoyl chloride, syn isomer, thus obtained is dissolved in methylene chloride (50 cc) and a 5.4 N solution of hydrogen chloride in ether (0.2 cc), and bromine (1.14 cc), are added to this solution at 20° C. The mixture is stirred for 20 hours at 20° C. and then concentrated to dryness at 20° C. under 20 mm Hg (2.7 kPa), and a brown oil (5.42 g) consisting principally of 4-bromo-2-methoxyimino-3-oxobutyryl chloride, syn isomer, is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04365062
Source datasetuspto-grants-1982_12
ORD IDord-bd4567e8e3fb4e0bafbde3ba28b1adc4
Source noteuspto-grants-1982_12