Sodium borohydride → HCID 67240522, compound
Reaction equation
[CH3:1][S:2][C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[O:8])=[C:5]([C:11]([F:14])([F:13])[F:12])[CH:4]=1.[BH4-].[Na+]>CO>[CH3:1][S:2][C:3]1[CH:10]=[CH:9][C:6]([CH2:7][OH:8])=[C:5]([C:11]([F:12])([F:13])[F:14])[CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4-Methylsulfanyl-2-trifluoromethyl-benzaldehyde (4.87 mmol) was dissolved in mL of MeOH and the resulting solution was treated with NaBH4 (221.1 mg, 5.84 mmol). The reaction mixture was stirred at room temperature for 2 h. The solvent was evaporated and the residue was partitioned between CH2Cl2 and 1N HCl solution. The combined extracts were washed with brine, dried over Na2SO4. A small portion of extracts was evaporated to afford the desired product.
Workup
- customThe solvent was evaporated
- customthe residue was partitioned between CH2Cl2 and 1N HCl solution
- washThe combined extracts were washed with brine
- dry with materialdried over Na2SO4
- customA small portion of extracts was evaporated
Sources & evidence
- ORD record
- ord-5f30dccde8eb43b3ae6fa2eae30fef58
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08426604B2
Reaction notes
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