HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophene → Cyclopentyl-2-thienylmethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Cyclopentanecarboxylic acid | HCID 18840 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Cyclopentanecarbonyl chloride | HCID 78284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Cyclopentyl-2-thienylmethanone | HCID 10219686 | — |
Reaction Steps
Cyclopentanecarboxylic acid chloride, prepared from 100 mmol cyclopentanecarboxylic acid and 120 mmol of thionyl chloride, was dissolved in 100 mL of methylene chloride, and the solution was cooled in an ice bath. Thiophene (13.4 mL, 100 mmol) and SnCl4 (25 mL of a 1M solution in methylene chloride) were added. The reaction was warmed to room temperature and stirred for 72 hours. The reaction was quenched with 1 N HCl, and the mixture was extracted with three portions of methylene chloride. The organic extract was washed with satd aqueous NaHCO3, was dried over MgSO4, and filtered through a pad of silica gel. The solvent was removed by rotary evaporation to give 12.28 g of crude product, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05597832 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-95d166eb65f54d5d9d07923bb23d65ab |
| Source note | uspto-grants-1997_01 |