Oxalyl chloride → 1,3-Dichloro-5,6-dihydro-4H-cyclopenta(c)thiophen-4-one

To a stirred solution of 3-(2,5-dichloro-3-thienyl)propanoic acid (5.0 g, 24.2 mmol) in CH2Cl2 (50 mL) was added oxalyl chloride (3.5 g, 27.5 mmol) and the mixture was heated at reflux temperature for 1 hour. After cooling, volatiles were removed by evaporation. To a stirred solution of the acid chloride in CH2Cl2 (125 mL) was added aluminum chloride (4.0 g, 30 mmol) at room temperature. After stirring for 20 min, aluminum chloride (4.5 g, 33.7 mmol) was added. The mixture was stirred for additional 1 hour at room temperature. The reaction mixture was poured into ice-water and the whole extracted with dichloromethane (100 mL×3). The combined organic layer was washed with brine (100 mL), dried over MgSO4 and concentrated in vacuo to give the subtitle compound as light yellow solids (4.52 g, 98% yield). The compound was used for next reaction without further purification.

1. temperaturethe mixture was heated
2. temperatureat reflux temperature for 1 hour
3. temperatureAfter cooling
4. customvolatiles were removed by evaporation
5. stirringThe mixture was stirred for additional 1 hour at room temperature
6. extractionthe whole extracted with dichloromethane (100 mL×3)
7. washThe combined organic layer was washed with brine (100 mL)
8. dry with materialdried over MgSO4
9. concentrationconcentrated in vacuo

ORD record

ord-dc2e82cc259245a1ab4a5a0c94fdbf03

Source dataset

uspto-grants-2000_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06048880