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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70242Generated: October 25, 2026

Trichloromethanesulfenyl chloride → 5-Chloro-3-(propan-2-yl)-1,2,4-thiadiazole

https://huagongshe.com/reaction/70242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloromethanesulfenyl chlorideHCID 11666—
ReactantSodium HydroxideHCID 14798—
Reactant2-Methylpropanimidamide hydrochlorideHCID 2782053—
SolventDichloromethaneHCID 6344—
Product5-Chloro-3-(propan-2-yl)-1,2,4-thiadiazoleHCID 1287468360.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 2-methyl propanimidamide hydrochloride (5.0 g, 40.8 mmol), trichloromethanesulfenyl chloride (7.14 g, 38.4 mmol) in methylene chloride (200 mL) at 0° C. was added dropwise an aqueous solution of sodium hydroxide (50%, 9.9 mL) over 20 minutes. The reaction mixture was stirred for 2 h at 0° C. and then was allowed to warm to room temperature, and stirred for an additional 3 h. Ice was added to the reaction mixture, the mixture was separated, and the aqueous layer was extracted with methylene chloride (3×25 mL). The combined organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by medium pressure liquid chromatography (0 to 100% gradient of ethyl acetate in hexanes as eluant) to provide the title compound as a oil (3.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822521B2
Source datasetuspto-grants-2014_09
ORD IDord-ea9f97223aea4491bd7056a3dd4b20cc
Source noteuspto-grants-2014_09