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3-(Trimethoxysilyl)propyl chloride → Acryloxypropyltrimethoxysilane

HRID 6275
Notes
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Reaction equation

HRID 6275 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-:16])(=[O:15])[CH:13]=[CH2:14].[K+]>>[C:12]([O:16][CH2:2][CH2:3][CH2:4][Si:5]([O:10][CH3:11])([O:8][CH3:9])[O:6][CH3:7])(=[O:15])[CH:13]=[CH2:14]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 624493-(Trimethoxysilyl)propyl chlorideHCID 4429391Potassium acrylate

Product 1

HCID 151204Acryloxypropyltrimethoxysilane

Procedure

Trichlorosilane and allyl chloride were subjected to hydrosilylation reaction in a solvent in the presence of a platinum catalyst, followed by esterification reaction with methanol and urea and further by distillation to obtain γ-chloropropyltrimethoxysilane. The thus obtained γ-chloropropyltrimethoxysilane and potassium acrylate were subjected to desalting in a solvent, followed by removal of potassium chloride. Subsequently, low boiling components including the solvent were distilled off under reduced pressure to obtain crude γ-acryloxypropyltrimethoxysilane having a purity of approximately 90%.

Workup

  1. customfollowed by removal of potassium chloride
  2. distillationwere distilled off under reduced pressure

Sources & evidence

ORD record
ord-d955b6bed1764bfcacbd148dda54d25f
Source dataset
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05247117

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes