HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Toluene → Nonamethyltetrasiloxanyl 2-methylprop-2-enoate

HRID 16037
Notes
Print preview

Reaction equation

HRID 16037 reaction equation
[CH3:1][Si:2]1([CH3:12])[O:7][Si:6]([CH3:9])([CH3:8])[O:5][Si:4]([CH3:11])([CH3:10])[O:3]1.[C:13]([O:18][Si:19](C)([CH3:21])[CH3:20])(=[O:17])[C:14]([CH3:16])=[CH2:15].[C:23]1(C)C=CC=CC=1>>[CH3:23][Si:2]([CH3:12])([CH3:1])[O:3][Si:4]([CH3:11])([CH3:10])[O:5][Si:6]([CH3:9])([CH3:8])[O:7][Si:19]([CH3:21])([CH3:20])[O:18][C:13](=[O:17])[C:14]([CH3:16])=[CH2:15]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 1140TolueneHCID 10914HexamethylcyclotrisiloxaneHCID 27338392-Propenoic acid, 2-methyl-, trimethylsilyl ester

Product 1

HCID 12991985Nonamethyltetrasiloxanyl 2-methylprop-2-enoate

Procedure

5 g of hexamethylcyclotrisiloxane, 3.5 g of trimethylsilyl methacrylate and 0.3 g of Amberlyst A15 resin catalyst were stirred in 2.5 ml of toluene. After 7 h at room temperature the catalyst was filtered and the solvent evaporated under reduced pressure to furnish nonamethyl-1-methacryloyloxy-tetrasiloxane.

Workup

  1. filtration
After 7 h at room temperature the catalyst was filtered
  • customthe solvent evaporated under reduced pressure
  • Sources & evidence

    ORD record
    ord-8709a273d055413f9e38955d2fe3c86e
    Source dataset
    uspto-grants-2010_06
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07736634B2

    Reaction notes

    Loading…

    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes