(4-Carboxybutyl)triphenylphosphonium bromide → HCID 13080736, compound

A suspension of (4-carboxy butyl) triphenyl phosphonium bromide (289.3 g, 652.6 mmol) in tetrahydrofuran (1000 ml) was cooled on ice. To the suspension, potassium t-butoxide (146.3 g, 1304 mmol) was added and the mixture was warmed to room temperature. A solution of (3aR,4S,5R,6aS)-4-(t-butyldimethylsilyloxymethyl)-5-(2-tetrahydropyranyloxy)hexahydrocyclopenta[b]furan-2-ol (23) (97.2 g, 261 mmol) in tetrahydrofuran (500 ml) was added, and the resulting solution was stirred for approximately 1.5 hours. Ice water (800 ml) was added to the reaction and the mixture was concentrated under reduced pressure. Then, ice-cooled 1N-hydrochloric acid (600 ml) and ethyl acetate (800 ml) were added to the residue and the mixture was stirred, let to stand and then separated into two layers. The aqueous layer was extracted twice with ethyl acetate (400 ml). The organic layers were combined, and washed with saturated aqueous sodium chloride (800 ml). After drying with anhydrous magnesium sulfate, the solution was concentrated under reduced pressure, diethyl ether (1400 ml) was added to the residue and the mixture was stirred for 30 minutes. The resulting mixture was filtered, and the deposited white solid was eliminated. The filtrate was concentrated under reduced pressure to give crude (Z)-7-[(1R,2S,3R,5S)-2-(t-butyldimethylsilyloxymethyl)-5-hydroxy-3-(2-tetrahydropyranyloxy)cyclopentyl]-5-heptenoic acid (24) (220 g) as white solid. The entire amount was used in the following step without purification.

1. temperaturewas cooled on ice
2. concentrationthe mixture was concentrated under reduced pressure
3. temperatureThen, ice-cooled 1N-hydrochloric acid (600 ml) and ethyl acetate (800 ml)
4. additionwere added to the residue
5. stirringthe mixture was stirred
6. customseparated into two layers
7. extractionThe aqueous layer was extracted twice with ethyl acetate (400 ml)
8. washwashed with saturated aqueous sodium chloride (800 ml)
9. dry with materialAfter drying with anhydrous magnesium sulfate
10. concentrationthe solution was concentrated under reduced pressure, diethyl ether (1400 ml)
11. additionwas added to the residue
12. stirringthe mixture was stirred for 30 minutes
13. filtrationThe resulting mixture was filtered
14. concentrationThe filtrate was concentrated under reduced pressure

ORD record

ord-16af6b3083bd42a3bff2050bea5716f0

Source dataset

uspto-grants-2012_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08236969B2