Hydrochloric Acid → alpha-(4-Methoxyphenyl)-1-(2-phenylethyl)-4-piperidinemethanol hydrochloride

HRID 1493193Notes

Reaction equation

HRID 1493193 reaction equation
[ClH:1].[CH3:2][O:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]([CH:12]2[CH2:17][CH2:16][N:15]([CH2:18][CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH2:14][CH2:13]2)=[O:11])=[CH:6][CH:5]=1.C[O-].[Na+].[BH4-].[Na+].Cl>CCO.CO.CCOC(C)=O>[ClH:1].[CH3:2][O:3][C:4]1[CH:5]=[CH:6][C:7]([CH:10]([CH:12]2[CH2:13][CH2:14][N:15]([CH2:18][CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH2:16][CH2:17]2)[OH:11])=[CH:8][CH:9]=1

Participants

7

Procedure

A solution of (4-methoxyphenyl)[1-(2-phenylethyl)-4-piperidinyl]-methanone hydrochloride (3.5 g, 9.7 mmol) in absolute EtOH (75 ml) was treated with sodium methoxide (0.53 g, 9.7 mmol) followed by sodium borohydride (1.08 g, 20 mmol) and the mixture stirred for 42 h at room temperature The reaction mixture was filtered and the filtrate concentrated to a solid residue which was dissolved in absolute Et2O and treated with HCl (9.7 mmol) dissolved in CH3OH/EtOAc (1:3, 8 ml). The resulting precipitate was filtered and recrystallized from CH3OH/Et2O to give alpha-(4-methoxyphenyl)-1-(2-phenylethyl)-4-piperidinemethanol hydrochloride, mp 162.5°-164° C.

Workup

  1. filtrationwas filtered
  2. concentrationthe filtrate concentrated to a solid residue which
  3. dissolutionwas dissolved in absolute Et2O
  4. filtrationThe resulting precipitate was filtered
  5. customrecrystallized from CH3OH/Et2O

Sources & evidence

ORD record
ord-57bd872fd1a04439902b5a920251547e
Source dataset
uspto-grants-1991_06
Patent number
US05021428

Reaction notes

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