HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 1-(5-Acetylthiophen-2-yl)propan-2-yl 4-methylbenzene-1-sulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 1-Thiophen-2-ylpropan-2-yl 4-methylbenzenesulfonate | HCID 254733 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(5-Acetylthiophen-2-yl)propan-2-yl 4-methylbenzene-1-sulfonate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04871755 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-e624b8d2984646e597475883f6ff052f |
| Source note | uspto-grants-1989_10 |