Hydrogen Peroxide → (R)-2-(3-Chloro-4-(methylsulfonyl)phenyl)-3-cyclopentylpropanoic acid

Temperatur

0 °C

A solution of lithium hydroxide (215 mg, 9.0 mmol) in water (2.8 mL) was treated with a 30% aqueous solution of hydrogen peroxide (2.0 mL, 18 mmol). This lithium hydroperoxide solution was cooled to 0° C. and was then slowly added to a solution of 4(R)-benzyl-3-[2(R)-(3-chloro-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionyl]-oxazolidin-2-one (2.20 g, 4.5 mmol) in tetrahydrofuran (18 mL) and water (5.8 mL) cooled to 0° C. The reaction was stirred at 0° C. for 1.5 h. At this time, the reaction was quenched with a 1.5N aqueous sodium sulfite solution (25 mL) and was further diluted with water (150 mL). This solution was extracted with diethyl ether (3×50 mL). The aqueous layer was then acidified to pH=2 with a 1N aqueous hydrochloric acid solution and extracted with ethyl acetate (3×50 mL). The organics were dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 75/25 hexanes/ethyl acetate plus 1% acetic acid) afforded 2(R)-(3-chloro-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionic acid (1.26 g, 85%) as a white solid: mp 106.1-108.8° C.; [α]23589=−43.0° (c=0.172, chloroform); EI-HRMS m/e calcd for C15H19ClO4S (M+) 330.0692, found 330.0690.

1. customAt this time, the reaction was quenched with a 1.5N aqueous sodium sulfite solution (25 mL)
2. additionwas further diluted with water (150 mL)
3. extractionThis solution was extracted with diethyl ether (3×50 mL)
4. extractionextracted with ethyl acetate (3×50 mL)
5. dry with materialThe organics were dried over sodium sulfate
6. filtrationfiltered
7. concentrationconcentrated in vacuo

ORD-Eintrag

ord-9fe486f1c1774687892f5a27f8d56de9

Quelldatensatz

uspto-grants-2003_03

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US06528543B1