Реакция #1742

ord-b0029680d3ec4bf2ada8460d535c1585

Уравнение реакции

CN(C)Cc1ccc(C2CCC(=O)CC2)cc1
4-(4-dimethylaminomethylphenyl)-cyclohexanone
[BH4-].[Na+]
sodium borohydride
CN(C)Cc1ccc([C@H]2CC[C@H](O)CC2)cc1
trans-4-(4-Dimethylaminomethylphenyl)-cyclohexanol

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеto react for 1.5 hours at ambient temperature
  2. 2
    Другоеevaporated down in vacuo
  3. 3
    workup.ADDITIONThe residue remaining is mixed with water
  4. 4
    workup.STIRRINGstirred for 30 minutes at ambient temperature
  5. 5
    Экстракцияextracted several times with chloroform
  6. 6
    СушкаThe combined extracts are dried with sodium sulphate
  7. 7
    Другоеevaporated down in vacuo
  8. 8
    workup.ADDITIONwhich consists of a mixture of trans/cis-4-(4-dimethylaminomethyl-phenyl)-cyclohexanol (cis fraction <10%)
  9. 9
    Другоеis purified by column chromatography (aluminium oxide neutral, activity stage III, ICN; petroleum ether/methylethyl ketone=5:1)
  10. 10
    ДругоеWhite crystals are obtained

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05726205uspto-grants-1998_03