Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165073Generated: October 30, 2026

Thionyl Chloride → 2-(1-Chloroethyl)-1,3-benzothiazole

https://huagongshe.com/reaction/2165073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant1-(1,3-Benzothiazol-2-yl)ethan-1-olHCID 2830674—
SolventDichloromethaneHCID 6344—
Product2-(1-Chloroethyl)-1,3-benzothiazoleHCID 10997958—

Reaction Steps

To a solution of 1-(2-benzothiazolyl)ethanol (2.5 g) prepared according to J. Indian Chem. Soc., 566 (1974) in methylene chloride (50 ml) was added thionyl chloride (3.32 g) and the resulting solution stirred at room temperature for 1 hour. The solution was poured onto ice-water (100 ml) and the organic extract separated. This extract was washed with aqueous bicarbonate (10 ml of a 5% solution) and then with water (50 ml). The methylene chloride layer was dried over anhydrous magnesium sulfate and evaporated to a light yellow oil (2.08 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939140
Source datasetuspto-grants-1990_07
ORD IDord-b7ea343a2c8946b4a3ba7c2e6a332844
Source noteuspto-grants-1990_07