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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261796Generated: November 2, 2026

Benzene → N-Butyl-N-(5-methyl-1,3,4-thiadiazol-2-yl)cyclopropanecarboxamide

https://huagongshe.com/reaction/261796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantTriethylamineHCID 8471—
ReactantCyclopropanecarbonyl chlorideHCID 77637—
ReactantHCID 70601298HCID 70601298—
ProductN-Butyl-N-(5-methyl-1,3,4-thiadiazol-2-yl)cyclopropanecarboxamideHCID 21315319—

Reaction Steps

N-(5-methyl-1,3,4-thiadiazol-2-yl)butylamine (1.7 g, 0.01 mole) in benzene (20 ml) was treated with triethylamine (1.53 ml) and cyclopropane carboxylic acid chloride (1.15 g). The reaction mixture was heated to reflux for 20 hours. The solution was then evaporated to dryness and the residue treated with ether and filtered. The solution was washed with water, dried and charcoaled, filtered and evaporated and the residue recrystallised from petrol ether (40°-60° C.) to give N-butyl-N-(5-methyl-1,3,4-thiadiazol-2-yl)cyclopropane carboxamide as a white crystalline solid. m.p. 82°-84° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04152442
Source datasetuspto-grants-1979_05
ORD IDord-77d3a3fef2e04f588e7aa672995c5ab3
Source noteuspto-grants-1979_05