反应 #1742
ord-b0029680d3ec4bf2ada8460d535c1585
反应方程式
溶剂
反应条件
后处理
- 1其他to react for 1.5 hours at ambient temperature
- 2其他evaporated down in vacuo
- 3workup.ADDITIONThe residue remaining is mixed with water
- 4workup.STIRRINGstirred for 30 minutes at ambient temperature
- 5萃取extracted several times with chloroform
- 6干燥The combined extracts are dried with sodium sulphate
- 7其他evaporated down in vacuo
- 8workup.ADDITIONwhich consists of a mixture of trans/cis-4-(4-dimethylaminomethyl-phenyl)-cyclohexanol (cis fraction <10%)
- 9其他is purified by column chromatography (aluminium oxide neutral, activity stage III, ICN; petroleum ether/methylethyl ketone=5:1)
- 10其他White crystals are obtained
实验过程
To a solution of 11.1 g (0.048 mol) of 4-(4-dimethylaminomethylphenyl)-cyclohexanone in 100 ml of absolute methanol, which has been cooled to -10° C., is added 1.82 g (0.048 mol) of sodium borohydride in batches with stirring. The reaction mixture is allowed to react for 1.5 hours at ambient temperature and then evaporated down in vacuo. The residue remaining is mixed with water, acidified with concentrated hydrochloric acid, stirred for 30 minutes at ambient temperature, made alkaline with 50% sodium hydroxide solution and extracted several times with chloroform. The combined extracts are dried with sodium sulphate and evaporated down in vacuo. The residue remaining, which consists of a mixture of trans/cis-4-(4-dimethylaminomethyl-phenyl)-cyclohexanol (cis fraction <10%) is purified by column chromatography (aluminium oxide neutral, activity stage III, ICN; petroleum ether/methylethyl ketone=5:1). White crystals are obtained, melting point 63°-65° C.