Tetrahydrofuran → 3-(3-bromophenyl)but-2-enoic acid

Temperature

50 °C

To a stirred mixture of 60% sodium hydride (2.01 g) in dry THF (100 mL) was added triethyl phosphonoacetate (10.1 mL) at 0° C. under nitrogen. The resulting mixture was added dropwise to a solution of 1-(3-bromophenyl)ethanone (10.0 g) in THF (100 mL) at reflux and the reaction heated at reflux overnight. The reaction mixture was diluted with water (300 mL), and extracted with dichloromethane (350 mL). The organic was dried (MgSO4), filtered and evaporated to afford a yellow oil. The oil was dissolved in methanol (100 mL), sodium hydroxide (6.03 g) and water (50 mL) added and the mixture was heated at 50° C. for 2 h. The reaction mixture was evaporated to leave an aqueous solution which was extracted twice with diethyl ether and the organic extracts were discarded. The aqueous solution was acidified with aqueous 2M HCl and then extracted with ethyl acetate (300 mL). The organic was dried (MgSO4), filtered and evaporated to afford the subtitle compound (11.70 g) as a solid.

1. temperatureat reflux
2. temperaturethe reaction heated
3. temperatureat reflux overnight
4. extractionextracted with dichloromethane (350 mL)
5. dry with materialThe organic was dried (MgSO4)
6. filtrationfiltered
7. customevaporated
8. customto afford a yellow oil
9. customThe reaction mixture was evaporated
10. customto leave an aqueous solution which
11. extractionwas extracted twice with diethyl ether
12. extractionextracted with ethyl acetate (300 mL)
13. dry with materialThe organic was dried (MgSO4)
14. filtrationfiltered
15. customevaporated

ORD record

ord-140d288c84cd4f809159ddb5b7e5cf1a

Source dataset

uspto-grants-2011_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08012980B2