Aluminium lithium hydride → [4'-(Methanesulfonyl)[1,1'-biphenyl]-3-yl]methanol
Reaction equation
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([C:17](OC)=[O:18])[CH:12]=2)=[CH:7][CH:6]=1)(=[O:4])=[O:3].[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[CH3:1][S:2]([C:5]1[CH:6]=[CH:7][C:8]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([CH2:17][OH:18])[CH:12]=2)=[CH:9][CH:10]=1)(=[O:3])=[O:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In an atmosphere of nitrogen, under ice-cooling, methyl 4′-(methylsulfonyl)biphenyl-3-carboxylate was added to a THF suspension of lithium aluminum hydride, followed by stirring for 20 minute to obtain [4′-(methylsulfonyl)biphenyl-3-yl]methanol.
Workup
- temperatureIn an atmosphere of nitrogen, under ice-cooling
Sources & evidence
- ORD record
- ord-5091657163d94514ae2854921c0f0b86
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07968552B2
Reaction notes
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