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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069200Generated: October 29, 2026

Dimethylamine → 2-benzyloxyimino-3-methoxyimino-N,N-dimethylbutyramide

https://huagongshe.com/reaction/1069200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantWaterHCID 962—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Benzyloxyimino-3-methoxyiminobutyric acidHCID 54001678—
CatalystDimethylformamideHCID 6228—
SolventTolueneHCID 1140—
Product2-benzyloxyimino-3-methoxyimino-N,N-dimethylbutyramideHCID 5445666153%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 0.9 g (3.6 mmol) of 2-benzyloxyimino-3-methoxyiminobutyric acid in 15 ml of toluene, 0.5 g (4.0 mmol) of thionyl chloride and one drop of N,N-dimethylformamide were added and the mixture was stirred for 1 hour at 60° C. After cooling with an ice, 5 ml of 50% dimethylamine solution was added and the mixture was stirred for 0.5 hour at room temperature. 30 ml of water was added and the mixture was extracted three times with 50 ml of diethylether. After washing with water and a saturated aqueous sodium chloride, the organic layer was dried over with anhydrous magnesium sulfate and the solvent was distilled off to obtain a residue, which was then purified by a column chromatography on a silica gel (n-hexane/ethyl acetate) to obtain 0.53 g (yield: 53%) of 2-benzyloxyimino-3-methoxyimino-N,N-dimethylbutyramide as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251949B1
Source datasetuspto-grants-2001_06
ORD IDord-abcb2cf2e4eb4c2494d9495d70b33a08
Source noteuspto-grants-2001_06