Methanol → HCID 11747608, compound
Reaction equation
[CH3:1][Si:2]([CH3:13])([CH2:4][Si:5](Cl)([Cl:11])[CH2:6][Si:7]([CH3:10])([CH3:9])[CH3:8])[CH3:3].[CH3:14][OH:15]>>[CH3:1][Si:2]([CH3:13])([CH2:4][Si:5]([Cl:11])([O:15][CH3:14])[CH2:6][Si:7]([CH3:10])([CH3:9])[CH3:8])[CH3:3]Participants
3
Conditions
- Temperature
- 70 °C
Procedure
13.7 g(50 mmoles) of 2,2,6,6-tetramethyl-4,4-dichloro-2,4,6-trisilaheptane were placed in the flask of the same set as Example 1, and then 1.8 g(60 mmoles) of dry methanol were added. The mixture was heated at 70° C. for 2 hrs. The amount of the product was 9.92 g and the yield 74%.
Sources & evidence
- ORD record
- ord-b6efa47268994222961eb742258b7bf6
- Source dataset
- uspto-grants-1994_04
- Patent number
- US05302734
Reaction notes
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