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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380100Generated: October 30, 2026

Ethyl bromoacetate → HCID 13590327, compound

https://huagongshe.com/reaction/1380100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantCarbonate IonHCID 19660—
ReactantHCID 13590326HCID 13590326—
SolventAcetoneHCID 180—
ProductHCID 13590327HCID 1359032715.7%

Reaction Steps

A mixture of 5-amino-6,7-dichloro-2-cyclopentyl-2,3-dihydro-2-methyl-1H-inden-1-one (800 mg), postassium carbonate (440 mg), and ethyl bromoacetate (540 mg) in acetone (20 ml) is heated at reflux overnight. The reaction mixture is filtered, the acetone is distilled at reduced pressure and the residual oil is dissolved in a mixture of ethanol (5 ml) and methylene chloride (5 ml) and treated with 10 N sodium hydroxide (2 ml). The mixture is stirred overnight, the solvents are distilled at reduced pressure and the residue is treated with water, then filtered and acidified with hydrochloric acid and extracted with ethyl acetate. Evaporation of the ethyl acetate gives 150 mg of [(6,7-dichloro-2-cyclo-pentyl-2,3-dihydro-2-methyl-1-oxo-1H-inden-5-yl)amino]acetic acid which melts at 199°-200° C. after recrystallization from chloroform-hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04579869
Source datasetuspto-grants-1986_04
ORD IDord-f7c128b9cf1e4c2cba6dc35946ed86fe
Source noteuspto-grants-1986_04