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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082982Generated: November 1, 2026

Benzene → HCID 54421021, compound

https://huagongshe.com/reaction/2082982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantPhosgeneHCID 6371—
ReactantEthyl 2-{[(chlorocarbonyl)oxy]imino}-3-oxobutanoateHCID 54491891—
ReactantHCID 178472877HCID 178472877—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Solventtert-ButanolHCID 6386—
ProductHCID 54421021HCID 54421021—

Reaction Steps

A solution of ethyl 2-hydroxyiminoacetoacetate (3.98 g.) and pyridine (1.98 g.) in benzene (25 ml.) was added dropwise to a solution of phosgene (2.48 g.) in benzene (30 ml.) for 30 minutes at 4° to 5° C. After stirring for 1 hour at the same temperature, the mixture was stirred for 1 hour at room temperature and allowed to stand overnight. A solution of tert-butyl alcohol (3.7 g.) and pyridine (3.96 g.) in benzene (25 ml.) was added dropwise for 30 minutes at 5° to 7° C. to the resultant solution containing ethyl 2-chlorocarbonyloxyiminoacetoacetate. After stirring for 1 hour at the same temperature, the reaction temperature was slowly elevated to room temperature, after which the mixture was stirred for 6 hours at the same temperature and allowed to stand overnight. A precipitate was dissolved by adding about the same volume of water as that of the organic layer to the reaction mixture. The aqueous layer was then separated. The organic layer was then washed with a 0.5M citric acid aqueous solution, a 5% sodium carbonate aqueous solution and a sodium chloride aqueous solution, and dried over magnesium sulfate. After drying, the solvent was distilled off to give ethyl 2-tert-butoxycarbonyloxyiminoacetoacetate (3.7 g.), oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04083848
Source datasetuspto-grants-1978_04
ORD IDord-bacef875938344ae8dac7e62acf14de4
Source noteuspto-grants-1978_04