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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609278Generated: November 1, 2026

Thionyl Chloride → Benzoyl chloride, 4-(hexyloxy)-

https://huagongshe.com/reaction/1609278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4-(Hexyloxy)benzoic acidHCID 70834—
ProductBenzoyl chloride, 4-(hexyloxy)-HCID 170235—

Reaction Steps

In 2 ml of thionyl chloride was dissolved 1.03 g of 4-hexyloxybenzoic acid and the solution was refluxed for 1 hour. The excess thionyl chloride was distilled off and the residue was dried in vacuo to give 4-hexyloxybenzoyl chloride. Separately, 1.00 g of 2-(2-aminophenylthio)benzonitrile and 0.89 g of triethylamine were dissolved in 10 ml of ether and while the solution was stirred with ice-cooling, a solution of the above 4-hexyloxybenzoyl chloride in 5 ml of ether was added. The mixture was stirred overnight. Next morning, water and an aqueous solution of sodium hydrogen carbonate were added in the order mentioned and the resulting precipitate was extracted with ethyl acetate. The extract was dried over magnesium sulfate, the solvent was distilled off, and the residue was recrystallized from ethyl acetate-n-hexane to give 1.27 g of the title compound as white prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399703
Source datasetuspto-grants-1995_03
ORD IDord-986e4d8a5c3042a1ab61fcb827496913
Source noteuspto-grants-1995_03