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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487550Generated: October 28, 2026

Triethylsilane → 3-Methyl-6-(2-bromoethyl)benzothiazolinone

https://huagongshe.com/reaction/487550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
Reactant3-Methyl-6-(bromoacetyl)benzothiazolinoneHCID 86746657—
SolventTrifluoroacetic acidHCID 6422—
Product3-Methyl-6-(2-bromoethyl)benzothiazolinoneHCID 70183836—

Reaction Steps

In a 500-cm3 ground-necked flask surmounted by a condenser and placed in an oil bath, 42.9 g (0.15 mol) of 3-methyl-6-(bromoacetyl)benzothiazolinone are dissolved in 77 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 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 cyclohexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05296477
Source datasetuspto-grants-1994_03
ORD IDord-b86df02b622a45e99c31a7d627b06611
Source noteuspto-grants-1994_03