HCID 826664, compound → HCID 54020792, compound

HRID 1443043Notes

Reaction equation

HRID 1443043 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH:10]2[CH2:15][CH2:14][N:13]([CH3:16])[CH2:12][CH2:11]2)=[O:9])=[CH:4][CH:3]=1.[BH4-].[Na+]>CO>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH:10]2[CH2:15][CH2:14][N:13]([CH3:16])[CH2:12][CH2:11]2)[OH:9])=[CH:4][CH:3]=1

Participants

4

Reactant 2

HCID 826664HCID 826664, compoundHCID 4311764Sodium borohydride

Product 1

HCID 54020792HCID 54020792, compoundYield 90%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a solution of 4-fluorophenyl 1-methylpiperidin-4-yl methanone 10.10 g (5 mmol) in 30 ml methanol was added in small portions sodium borohydride 0.378 g (10 mmol). The reaction mixture was stirred at room temperature for two hours, concentrated, added water and extracted with methylene chloride 2×50 ml. The combined organic solution was dried over sodium sulfate and concentrated to give 1.0 g of desired product in 90% yield.

Workup

  1. concentrationconcentrated
  2. additionadded water
  3. extractionextracted with methylene chloride 2×50 ml
  4. dry with materialThe combined organic solution was dried over sodium sulfate
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-9c916751d7944b03b3ddc3840c7c4dd7
Source dataset
uspto-grants-2010_02
Patent number
US07659395B2

Reaction notes

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