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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487547Generated: October 24, 2026

Triethylsilane → 6-(2-Bromoethyl)benzothiazolone

https://huagongshe.com/en/reaction/487547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
Reactant6-(Bromoacetyl)benzothiazolinoneHCID 131717829—
SolventTrifluoroacetic acidHCID 6422—
Product6-(2-Bromoethyl)benzothiazoloneHCID 69227973—

Reaction Steps

In a 500-cm3 ground-necked flask surmounted by a condenser, and placed in an oil bath, 40.8 g (0.15 mol) of 6-(bromoacetyl)benzothiazolinone are dissolved in 90 cm3 of trifluoroacetic acid with magnetic stirring and while the temperature is stabilized at 60° C. 52.7 cm3 (0.33 mol) of triethylsilane are introduced dropwise via a dropping funnel. After the addition, the heating is stopped and the mixture is then left stirring vigorously for 30 hours. The reaction medium is hydrolyzed by pouring it into ice-cold water, and the precipitate obtained is drained and washed with water until the filtrate is neutral and then with hexane. The product is dried and recrystallized in absolute ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05296477
Source datasetuspto-grants-1994_03
ORD IDord-730a0c86cd8e45cabbb5f4a71d7944fa
Source noteuspto-grants-1994_03