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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156957Generated: November 1, 2026

4-Toluenesulfonyl chloride → HCID 12917757, compound

https://huagongshe.com/reaction/1156957

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant4,5,6,7-Tetrahydro-4-benzothiazolemethanolHCID 12917751—
SolventPyridineHCID 1049—
ProductHCID 12917757HCID 1291775772%

Reaction Conditions

Temperature10 °C

Reaction Steps

9.95 g (52 mmoles) p-toluenesulfonyl chloride are added portionwise to a mixture of 8 g (47 mmoles) of the above derivative (IV) and 15 g anhydrous pyridine, while maintaining the temperature at 10° C. After stirring for 24 hrs at room temperature, the mixture is hydrolyzed and is then extracted with ethyl acetate. The combined organic phases are washed with water, dried and evaporated. The residual oil crystallizes slowly. The product is recristallyzed from boiling isopropyl oxide, on cooling. Yield: 72%. M.p.=64°-65° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04337343
Source datasetuspto-grants-1982_06
ORD IDord-6701af09dfcc4b22a3ee40cfa5444a7e
Source noteuspto-grants-1982_06