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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260833Generated: October 26, 2026

Ethyl 4-bromobutyrate → Ethyl 4-(3-benzyloxycarbonyl-1-indolyl)-butyrate

https://huagongshe.com/reaction/260833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-bromobutyrateHCID 76300—
Reactantbenzyl 1H-indole-3-carboxylateHCID 8605861—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-(3-benzyloxycarbonyl-1-indolyl)-butyrateHCID 22400494—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of benzyl indole-3-carboxylate, ethyl 4-bromobutyrate and potassium t-butoxide in N,N-dimethylformamide was stirred at 50° C. for 4 hours. After insoluble materials were filtered off, the filtrate was diluted with ethyl acetate, and washed with diluted hydrochloric acid and water, dried over magnesium sulfate and concentrated. The concentrate was chromatographed on a silica gel column to give the object compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05530019
Source datasetuspto-grants-1996_06
ORD IDord-bea85c6851bd439881b44c9c5a4c9fcc
Source noteuspto-grants-1996_06