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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325977Generated: October 27, 2026

Chloroacetonitrile → [(5-Chloro-1,3-benzothiazol-2-yl)sulfanyl]acetonitrile

https://huagongshe.com/reaction/325977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantTriethylamineHCID 8471—
ReactantHCID 178527796HCID 178527796—
SolventTolueneHCID 1140—
Product[(5-Chloro-1,3-benzothiazol-2-yl)sulfanyl]acetonitrileHCID 13312471—

Reaction Steps

51.0 g (0.254 m), 5-chloro-2-mercaptobenzothiazole, 22.8 g (0.304 m) chloroacetonitrile and 30.7 g triethylamine are dissolved in 600 ml of toluene and the solution is heated to reflux for 3 hr, then allowed to cool to room temperature. The toluene solution is washed with water, dried over anhydrous magnesium sulfate and treated with Darco. After the solvent is removed, the residual solid is recrystallized from 300 ml. benzene. The recovered material is recrystallized from cyclohexane. A total yield of 52 g (86%) is obtained. The recrystallized sample has a melting point of 96°-7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04443606
Source datasetuspto-grants-1984_04
ORD IDord-f11a01adcb744535b2e4d99644d3bd84
Source noteuspto-grants-1984_04