Sodium borohydride → HCID 14257858, compound

HRID 1681086Notes

Reaction equation

HRID 1681086 reaction equation
[C:1]1([CH2:7][CH2:8][N:9]2[CH2:14][CH2:13][CH:12]([C:15]([C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([C:23]([F:26])([F:25])[F:24])[CH:18]=3)=[O:16])[CH2:11][CH2:10]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[BH4-].[Na+]>CO>[C:1]1([CH2:7][CH2:8][N:9]2[CH2:14][CH2:13][CH:12]([CH:15]([C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([C:23]([F:26])([F:24])[F:25])[CH:18]=3)[OH:16])[CH2:11][CH2:10]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

4

Reactant 2

HCID 4311764Sodium borohydrideHCID 14257846HCID 14257846, compound

Product 1

HCID 14257858HCID 14257858, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a solution of [1-(2-phenylethyl)-4-piperidinyl][3-(trifluoromethyl)-phenyl]-methanone (2.8 g, 7.75 mmol) in methanol (50 ml) cooled in an ice bath was added portionwise sodium borohydride (0.3 g, 7.75 mmol). The reaction was allowed to warm to room temperature and stirred an additional 4 h. The mixture was evaporated and the residue extracted with Et2O, washed with H2O (3×100 ml), saturated aqueous NaCl (1×100 ml), dried (Mg SO4), filtered and evaporated to give a white solid. This solid was recrystallized from ether-hexane to give white needles, mp 143°-147° C.

Workup

  1. customThe mixture was evaporated
  2. extractionthe residue extracted with Et2O
  3. washwashed with H2O (3×100 ml), saturated aqueous NaCl (1×100 ml)
  4. dry with materialdried (Mg SO4)
  5. filtrationfiltered
  6. customevaporated
  7. customto give a white solid
  8. customThis solid was recrystallized from ether-hexane
  9. customto give white needles, mp 143°-147° C.

Sources & evidence

ORD record
ord-2cc93bb9d8a94ac09e07a77729d67af7
Source dataset
uspto-grants-1992_12
Patent number
US05169096

Reaction notes

Loading…