Water → HCID 66750495, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9](=[O:13])[CH:8]([CH3:14])[CH2:7][CH2:6]2.[BH4-].[Na+].O>CO>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]([OH:13])[CH:8]([CH3:14])[CH2:7][CH2:6]2Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To an ice-cooled solution of 6-methoxy-2-methyl-3,4-dihydro-2H-naphthalen-1-one (7.0 g, 36.8 mmol) in MeOH (120 mL) is added NaBH4 (2.78 g, 73.6 mmol) portion wise and the mixture is stirred at RT for 20 min. Then the reaction is poured to 120 mL of water and extracted with ether. The organic phase is dried with MgSO4, concentrated to give the title compound as a light yellow oil and it is used in the next step without purification.
Workup
- extractionextracted with ether
- dry with materialThe organic phase is dried with MgSO4
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-05bd5e8748984941a461d387e32a9b1b
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07700633B2
Reaction notes
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