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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2350927Generated: November 3, 2026

Acetyl chloride → 1-(5-Acetylthiophen-2-yl)propan-2-yl 4-methylbenzene-1-sulfonate

https://huagongshe.com/reaction/2350927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant1-Thiophen-2-ylpropan-2-yl 4-methylbenzenesulfonateHCID 254733—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product1-(5-Acetylthiophen-2-yl)propan-2-yl 4-methylbenzene-1-sulfonateHCID 23323905—

Reaction Steps

2-(p-Toluenesulphonyloxy)-propylthiophene was reacted with acetyl chloride and aluminium trichloride in methylene chloride to give 5-acetyl-2-(p-toluenesulphonyloxy)-propylthiophene. With sodium azide in DMSO there was obtained therefrom 5-(3-azidopropyl)-2-thienyl methyl ketone. Oxidation with sodium hypobromite gave 5-(3-azidopropyl)-2-thiophenecarboxylic acid, m.p. 71°-72°. Reaction of this acid with thionyl chloride and subsequent treatment with conc. ammonia yielded 5-(3-azidopropyl)-2-thiophenecarboxamide, m.p. 85°-87°. There was obtained therefrom after treatment with triphenylphosphine and hydrolysis 5-(3-aminopropyl)-2-thiophenecarboxamide, m.p. 143.5°-144° (from water).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871755
Source datasetuspto-grants-1989_10
ORD IDord-e624b8d2984646e597475883f6ff052f
Source noteuspto-grants-1989_10