Hydrogen Peroxide → HCID 19039150, compound
Reaction equation
[CH2:1]([Si:4]([CH2:16][CH:17]=[CH2:18])([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH2:5][CH2:6][CH2:7][CH2:8][CH3:9])[CH:2]=[CH2:3].[BH4-].[Na+].[OH-:21].[Na+].[OH:23]O>O1CCCC1>[OH:21][CH2:3][CH2:2][CH2:1][Si:4]([CH2:16][CH2:17][CH2:18][OH:23])([C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)[CH2:5][CH2:6][CH2:7][CH2:8][CH3:9]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
50 g of boron trifluoride ether complex was dripped into a mixed solution of 100 g of diallylphenyl-n-pentylsilane, 9.6 g of sodium borohydride and 500 g of tetrahydrofuran. After the reaction mixture was stirred for 4 hours at room temperature, a 300 ml aqueous solution of 20% sodium hydroxide and then a 100 ml aqueous solution of 30% hydrogen peroxide were dripped into the mixture. After an overnight stirring were dripped into the mixture. After an overnight stirring at room temperature, extraction was conducted using ethyl acetate. Following conventional washing and concentration procedures, 120 g of di(3-hydroxypropyl)phenyl-n-pentylsilane was obtained. IR (liquid film) νmax: 3030 (s, br), 2920 (s), 2870 (s), 1420 (m), 1105 (s), 1050 (s), 1005 (s) and 850 (m) cm-1
Workup
- stirringAfter an overnight stirring
- stirringAfter an overnight stirring at room temperature
- extractionextraction
- washFollowing conventional washing
- concentrationconcentration procedures
Sources & evidence
- ORD record
- ord-2c3ac107422747b19c9cb9141b78f4e5
- Source dataset
- uspto-grants-1997_06
- Patent number
- US05641431
Reaction notes
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