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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843595Generated: October 27, 2026

Trichloromethanethiol → 5-Chloro-3-p-tolyl-[1,2,4]thiadiazole

https://huagongshe.com/reaction/843595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloromethanethiolHCID 6390—
ReactantTriethylamineHCID 8471—
Reactant4-Methylbenzene-1-carboximidamide hydrochlorideHCID 122753—
SolventChloroformHCID 6212—
Product5-Chloro-3-p-tolyl-[1,2,4]thiadiazoleHCID 2261106644%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a mixture of p-methylbenzamidine hydrochloride (5.1 g, 30.0 mmol) in CHCl3 (100 ml) is added triethyl amine (15.12 g, 20.9 ml, 150.0 mmol) and cooled to 5° C. in an ice-water bath. To the mixture is slowly added perchloromethyl mercaptan (95%, 6.16 g, 31.5 mmol) in CHCl3(10 ml) over 1 hour. The yellow solution is allowed to warm up to room temperature. After 2 hours the mixture is washed with water (100 ml×2) and brine (100 ml). The organic layer is dried over MgSO4 and the solvent is removed under reduced pressure to yield a brown oil. The oil is purified on a bed of silica gel, eluting with 1:1 CHCl3:hexanes to yield 3-(p-tolyl)-5-chloro-1,2,4-thiadiazole as a yellow solid (2.78 g, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380187B2
Source datasetuspto-grants-2002_04
ORD IDord-be99e0bc80fc484f861a3e904e98a3c2
Source noteuspto-grants-2002_04