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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273842Generated: November 1, 2026

Triethylsilane → 1-[5-(2-Bromopropyl)-2,3-dihydro-1H-indol-1-yl]ethanone

https://huagongshe.com/reaction/273842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantHCID 20094393HCID 20094393—
SolventTrifluoroacetic acidHCID 6422—
Product1-[5-(2-Bromopropyl)-2,3-dihydro-1H-indol-1-yl]ethanoneHCID 2009437076.5%

Reaction Steps

To a solution of 1-acetyl-5-(2-bromopropionyl)indoline (210 g) in trifluoroacetic acid (700 ml) was added triethylsilane (190 g) over a period of 30 minutes with stirring under ice cooling, the mixture was stirred for 30 minutes under ice cooling, and then for 1 hour at room temperature. After the reaction mixture was concentrated under reduced pressure, the residue was poured into water (2 l), and to the mixture was added hexane (500 ml) and stirred. The precipitates were collected by filtration, washed with hexane, and recrystallized from ethyl acetate-hexane to give 153 g of 1-acetyl-5-(2-bromopropyl)indoline melting at 124°-126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387603
Source datasetuspto-grants-1995_02
ORD IDord-6db7ef8e56644148954d7d9b13f4e8bb
Source noteuspto-grants-1995_02