Potassium Hydroxide → (R)-4-(4-Fluoro-3-methyl-phenyl)-4-hydroxy-butanoic acid

To a solution of (R)-Methyl 4-(4-fluoro-3-methylphenyl)-4-hydroxybutanoate (181 mg, 0.80 mmol) in 5 mL dioxane was added 5 mL aqueous 5% KOH at 25° C. The mixture was stirred for 30 min at room temperature and then the reaction quenched by the addition of 10 mL of 1M HCl and the resulting mixture extracted with ethyl acetate (2×10 mL). The combined organic layers were extracted with 5% K2CO3 (3×5 mL) and the aqueous extracts acidified with 1M HCl to pH3. The resulting white colloidal suspension was extracted with ethyl acetate (3×20 mL) and the combined organic layers washed with brine (2×15 mL) before being dried over Na2SO4. The solvent was evaporated under reduced pressure and the crude product (233 mg) was used in the next step without further purification.

1. customthe reaction quenched by the addition of 10 mL of 1M HCl
2. extractionthe resulting mixture extracted with ethyl acetate (2×10 mL)
3. extractionThe combined organic layers were extracted with 5% K2CO3 (3×5 mL)
4. extractionThe resulting white colloidal suspension was extracted with ethyl acetate (3×20 mL)
5. washthe combined organic layers washed with brine (2×15 mL)
6. dry with materialbefore being dried over Na2SO4
7. customThe solvent was evaporated under reduced pressure
8. customthe crude product (233 mg) was used in the next step without further purification

ORD record

ord-e450c335c68e4a2782b4e80d4c507df8

Source dataset

uspto-grants-2012_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08119692B2