Water → HCID 22016388, compound
Reaction equation
[CH2:1]=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH:7]([Si:9]([CH3:12])([CH3:11])Cl)[CH3:8].C(N(CC)CC)C.[OH2:20]>CCOCC>[CH2:1]=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH:7]([Si:9]([CH3:12])([CH3:11])[OH:20])[CH3:8]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 7-oct-1-enyldimethylchlorosilane (2.56 ml) in ether (2 ml) was added dropwise over 1 hour to a stirring mixture of triethylamine (1.5 ml), water (0.18 ml) and ether (15 ml) in an ice/water bath. The resultant was stirred a further 1 hour in the ice/water bath and filtered washing the filtered solid with ether (10 ml). The filtrate was evaporated with a rotary evaporator and the residue partitioned between hexane (30 ml) and water (30 ml). The organic layer was separated, dried (MgSO4) and filtered through silica gel (70-230 mesh, 60 Å), washing with hexane (100 ml). The filtrate was evaporated with a rotary evaporator to afford a colorless oil which was vacuum dried and weighed (1.06 g).
Workup
- filtrationfiltered
- washwashing the filtered solid with ether (10 ml)
- customThe filtrate was evaporated with a rotary evaporator
- customthe residue partitioned between hexane (30 ml) and water (30 ml)
- customThe organic layer was separated
- dry with materialdried (MgSO4)
- filtrationfiltered through silica gel (70-230 mesh, 60 Å)
- washwashing with hexane (100 ml)
- customThe filtrate was evaporated with a rotary evaporator
- customto afford a colorless oil which
- customdried
Sources & evidence
- ORD record
- ord-a81c15de1d8f43258bed1055f2a37e2d
- Source dataset
- uspto-grants-1998_10
- Patent number
- US05824799
Reaction notes
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