反应详情

温度

-10 °C

Dissolve 4-[4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl]-α,α-dimethylbenzeneacetic acid, methyl ester hydrochloride (550 mg, 1.00 mmol) in methanol (5 mL) and add sodium borohydride (62.8 mg) in three batches. Stir for 1 hour, add 50% aqueous sodium hydroxide (800 mg) and heat to reflux with stirring. After 3 hours, cool to −10° C., add approximately 1.5 mL of 6N HCl over 10 minutes, filter the solid and wash with ice water (12 mL) such that the final filtrate is pH=5. Dry the resulting solid in vacuo (50-60° C., 10−1 mm) overnight to give the title compound (515 mg, 94%); mp 165-180° C.

1. temperatureheat
2. temperatureto reflux
3. stirringwith stirring
4. waitAfter 3 hours
5. filtrationfilter the solid
6. washwash with ice water (12 mL) such that the final filtrate
7. customDry the resulting solid in vacuo (50-60° C., 10−1 mm) overnight