3-(Trimethoxysilyl)propyl chloride → 3-(Trimethoxysilyl)propyl methacrylate

HRID 1436936Notes

Reaction equation

HRID 1436936 reaction equation
Cl[CH2:2][CH2:3][CH2:4][Si:5]([O:10][CH3:11])([O:8][CH3:9])[O:6][CH3:7].[C:12]([O-:17])(=[O:16])[C:13]([CH3:15])=[CH2:14].[K+]>C(P(CCCC)CCCC)CCC.C1C2NC3C(=CC=CC=3)SC=2C=CC=1>[C:12]([O:17][CH2:2][CH2:3][CH2:4][Si:5]([O:10][CH3:11])([O:8][CH3:9])[O:6][CH3:7])(=[O:16])[C:13]([CH3:15])=[CH2:14]

Participants

5

Reactant 2

HCID 624493-(Trimethoxysilyl)propyl chlorideHCID 23667354Potassium methacrylate2×

Product 1

HCID 173183-(Trimethoxysilyl)propyl methacrylateYield 89%

Reagents, catalysts & solvents 2

HCID 7108PhenothiazineCatalystHCID 13831TributylphosphineCatalyst

Procedure

Using a method analogous to Example 1, 198.7 g (1 mol) of 3-chloropropyltrimethoxysilane are reacted in the presence of 6.1 g (0.03 mol) of tri-n-butylphosphine and 0.1 g of phenothiazine with 130.4 g (1.05 mol) of potassium methacrylate at 90° C. The reaction is complete 10 hours after all the potassium methacrylate has been introduced. Work-up gives 221.0 g (89%) of 3-methacryloxypropyltrimethoxysilane having a purity of 98.3%.

Sources & evidence

ORD record
ord-e5e88907722f402fb7ea4e1aefb25a39
Source dataset
uspto-grants-2009_11
Patent number
US07619108B2

Reaction notes

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