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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660318Generated: November 2, 2026

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

https://huagongshe.com/reaction/1660318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
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

2 drops of dimethylformamide are added to a solution, at 20° C., of 2-methoxyimino-3-oxo-butyric acid (syn isomer) (4.08 g) in diethyl ether (50 cc), and oxalyl chloride (2 cc) dissolved in ethyl ether (5 cc) is then added dropwise in the course of 15 minutes. The mixture is stirred for 1 hour at 20° C., a further drop of dimethylformamide is added, and the reaction is continued for 15 minutes. The mixture is then 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 off, 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 is then concentrated to dryness at 20° C. under 20 mm Hg (2.7 kPa), and a brown oil consisting principally of 4-bromo-2-methoxyimino-3-oxo-butyryl chloride (syn isomer) (5.42 g) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307116
Source datasetuspto-grants-1981_12
ORD IDord-5e0c33385cdf4976aa8b03299f3a93bd
Source noteuspto-grants-1981_12