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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614212Generated: October 26, 2026

Triethylsilane → 6-(2-Bromoethyl)benzothiazolone

https://huagongshe.com/reaction/1614212

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 numberUS05196434
Source datasetuspto-grants-1993_03
ORD IDord-8e41478df04c4b148755e88107bd3e4f
Source noteuspto-grants-1993_03