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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615539Generated: October 29, 2026

4-Chloro-2-methylbutanoyl chloride → HCID 20407025, compound

https://huagongshe.com/reaction/615539

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-methylbutanoyl chlorideHCID 13770582—
Reactant3-tert-Butyl-1,2-thiazol-5-amineHCID 15117013—
SolventTolueneHCID 1140—
ProductHCID 20407025HCID 2040702512%

Reaction Steps

To a solution of 2.4 g of 3-(1,1-dimethylethyl)-5-aminoisothiazole dissolved in 150 ml of toluene under nitrogen was added 2.3 g of 2-methyl-4-chlorobutyric acid chloride. The reaction mixture was refluxed for about 24 hours and cooled. The solvent was evaporated under reduced pressure, and the product was isolated from the residue by chromatography over silica gel eluting with an ethyl acetate/Skellysolve B solvent mixture. Fractions containing the major component were combined and the solvent was evaporated therefrom to afford, following crystallization from toluene/Skellysolve B, 0.5 g of 4-chloro-N-[3-(1,1-dimethylethyl)-5-isothiazolyl]-2-methylbutanamide. Yield 12%. mp 144°-146° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04500343
Source datasetuspto-grants-1985_02
ORD IDord-14ad40eb1f5c42d68853b51b8b3743d4
Source noteuspto-grants-1985_02