Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([OH:10])[CH:9]=1)[CH:5]=[O:6].[C:11]([Si:15](Cl)([CH3:17])[CH3:16])([CH3:14])([CH3:13])[CH3:12]>>[Si:15]([O:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([O:10][Si:15]([C:11]([CH3:14])([CH3:13])[CH3:12])([CH3:17])[CH3:16])[CH:9]=1)[CH:5]=[O:6])([C:11]([CH3:14])([CH3:13])[CH3:12])([CH3:17])[CH3:16]Participants
3
Procedure
Prepared as in Example 12-1c from 3,5-dihydroxybenzaldehyde and tert-butylchlorodimethylsilane. Yield 100%, yellowish liquid. MS 267 (MH+).
Sources & evidence
- ORD record
- ord-4b3ce7b7e65e4d2a88e91f7ac0651156
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08076491B2
Linked notes
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