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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154111Generated: October 26, 2026

Dimethylformamide → Ethyl 2-(2-benzoyloxyethoxyimino)-3-oxobutyrate

https://huagongshe.com/reaction/1154111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromoethyl BenzoateHCID 523090—
ReactantHCID 178472877HCID 178472877—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(2-benzoyloxyethoxyimino)-3-oxobutyrateHCID 5376583592.4%

Reaction Steps

A mixture of ethyl 2-hydroxyimino-3-oxobutyrate (syn isomer, 15.7 g.), 2-bromoethyl benzoate (27.5 g.), potassium carbonate (20.7 g.), N,N-dimethylformamide (25 ml.) and ethyl acetate (25 ml.) was stirred at room temperature for 4 hrs. The reaction mixture was treated in a conventional manner to give ethyl 2-(2-benzoyloxyethoxyimino)-3-oxobutyrate (syn isomer, 28 g.). (2) A solution of ethyl 2-(2-benzoyloxyethoxyimino)-3-oxobutyrate (syn isomer, 28 g.), sulfuryl chloride (13.5 g.) and acetic acid (30 ml.) was stirred at 40° C. for 10 minutes and at room temperature for 5.5 hrs. The reaction mixture was treated in a conventional manner to give ethyl 2-(2-benzoyloxyethoxyimino)-4-chloro-3-oxobutyrate (syn isomer, 29 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04487767
Source datasetuspto-grants-1984_12
ORD IDord-b1dc8f0ad8da4a989d8c393cd6b3d625
Source noteuspto-grants-1984_12