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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857716Generated: October 27, 2026

Ethyl Acetate → 2-benzyloxy-N-methyl-N-(3-methyl-2-oxobutyl)acetamide

https://huagongshe.com/reaction/1857716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantBenzyloxyacetyl chlorideHCID 177085—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Methyl-1-(methylamino)butan-2-oneHCID 22130554—
SolventWaterHCID 962—
Product2-benzyloxy-N-methyl-N-(3-methyl-2-oxobutyl)acetamideHCID 2213091242%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 6.1 g (52.9 mmol) of 3-methyl-1-methylamino-2-butanone, 70.0 ml of ethyl acetate and 41.0 ml of water was stirred at 0° C. Added was 7.1 g (84.6 mmol) of sodium hydrogen carbonate, and the mixture was stirred for 10 minutes. There was added 8.5 ml (54.0 mmol) of benzyloxyacetylchloride over 30 minutes. After stirring at room temperature for 10 hours, the ethyl acetate layer was seperated, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The crude product was purified by silica gel chromatography (hexane/ethyl acetate 1:1) to give 5.8 g of 2-benzyloxy-N-methyl-N-(3-methyl-2-oxobutyl)-acetamide (18a') (yield 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147097
Source datasetuspto-grants-2000_11
ORD IDord-90bd613fa49943bfbe4bf0929ac19370
Source noteuspto-grants-2000_11