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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374788Generated: November 2, 2026

Ethyl bromoacetate → HCID 86599795, compound

https://huagongshe.com/reaction/1374788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant3-[(4-chlorophenyl)thio]-2,5-dimethyl-1H-indoleHCID 21077832—
SolventDimethylformamideHCID 6228—
ProductHCID 86599795HCID 86599795—

Reaction Steps

A stirred solution of 3-[(4-chlorophenyl)thio]-2,5-dimethyl-1H-indole (300 mg) in dry N,N-dimethylformamide (15 ml) was treated with sodium hydride (42 mg of a 60% dispersion in mineral oil). After 10 minutes the reaction was treated with ethyl bromoacetate (116 μl) and stirring continued for 24 hours. The reaction was poured into distilled water (200 ml) and extracted with diethyl ether (3×100 ml). The extracts were dried (MgSO4), evaporated in vacuo and the residue purified by flash column chromatography eluting with 10% ethyl acetate in iso-hexane. The subtitle compound was obtained as a yellow solid (yield 130 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166607B2
Source datasetuspto-grants-2007_01
ORD IDord-c65a9324bca948b085578e1e8f798c08
Source noteuspto-grants-2007_01