Methanol → HCID 131729537, compound
Reaction equation
[C:1]([SiH2:5][O:6][C:7]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH:8]1[O:12][C@@H:11]([C:13]#N)[CH2:10][CH2:9]1)([CH3:4])([CH3:3])[CH3:2].[CH3:27][O-:28].[Na+].C[OH:31]>>[CH3:27][O:28][C:13]([C@H:11]1[CH2:10][CH2:9][CH:8]([C:7]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[O:6][SiH2:5][C:1]([CH3:4])([CH3:3])[CH3:2])[O:12]1)=[O:31]Participants
4
Procedure
(R)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-2-carbonitrile was treated with sodium methoxide in MeOH to afford (R)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-2-carboxylic acid methyl ester.
Sources & evidence
- ORD record
- ord-d3411d37829d472eab431e297713df0e
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08148380B2
Reaction notes
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