تفاعل #1742

ord-b0029680d3ec4bf2ada8460d535c1585

معادلة التفاعل

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

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىto react for 1.5 hours at ambient temperature
  2. 2
    أخرىevaporated 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
    استخلاصextracted several times with chloroform
  6. 6
    تجفيفThe combined extracts are dried with sodium sulphate
  7. 7
    أخرىevaporated down in vacuo
  8. 8
    workup.ADDITIONwhich consists of a mixture of trans/cis-4-(4-dimethylaminomethyl-phenyl)-cyclohexanol (cis fraction <10%)
  9. 9
    أخرىis purified by column chromatography (aluminium oxide neutral, activity stage III, ICN; petroleum ether/methylethyl ketone=5:1)
  10. 10
    أخرىWhite crystals are obtained

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726205uspto-grants-1998_03