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Ethylene Oxide → Bisphenol A diglycidyl ether

HRID 25352
Notes
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Reaction equation

HRID 25352 reaction equation
[C:1]([O-:5])(=O)[CH:2]=[CH2:3].[CH2:6](O)[CH2:7][O:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][O:14][CH2:15][CH2:16]O.C1OC1.[CH2:22]1[O:25][CH:23]1[CH3:24].[OH:26][C:27]1[CH:32]=[CH:31][C:30]([C:33]([C:36]2[CH:41]=CC(O)=[CH:38][CH:37]=2)([CH3:35])[CH3:34])=[CH:29][CH:28]=1>>[CH3:35][C:33]([C:30]1[CH:31]=[CH:32][C:27]([O:26][CH2:3][CH:2]2[O:5][CH2:1]2)=[CH:28][CH:29]=1)([C:36]1[CH:41]=[CH:16][C:15]([O:14][CH2:13][CH:12]2[O:11][CH2:10]2)=[CH:38][CH:37]=1)[CH3:34].[CH:23]([O:25][CH2:22][CH2:15][O:14][CH2:13][CH2:12][O:11][CH2:10][CH2:9][O:8][CH:7]=[CH2:6])=[CH2:24]
ParticipantsProcedureSources & evidenceReaction notes

Participants

7

Reactant 5

HCID 6354Ethylene Oxide2×HCID 6378Propylene Oxide2×HCID 6623Bisphenol AHCID 8200Tetraethylene GlycolHCID 25188Acrylate3×

Product 2

HCID 2286Bisphenol A diglycidyl ether
HCID 3033992
Triethylene glycol divinyl ether

Procedure

Given as examples of the polymerizable polyfunctional vinyl monomers are the following acrylate compounds: trimethylolpropane tri(meth)acrylate, pentaerythritol tri(meth)acrylate, ethylene glycol di(meth)acrylate, tetraethylene glycol di(meth) acrylate, polyethylene glycol di(meth) acrylate, 1,4-butanediol di(meth)acrylate, 1,6-hexanediol di(meth)acrylate, neopentyl glycol di(meth)acrylate, trimethylolpropanetrioxyethyl (meth)acrylate, tris(2-hydroxyethyl)isocyanurate tri(meth)acrylate, tris(2-hydroxyethyl)isocyanurate di(meth)acrylate, bis(hydroxymethyl)tricyclodecane di(meth)acrylate, di(meth)acrylate of a diol which is an addion compound of ethylene oxide or propylene oxide to bisphenol A, di(meth)acrylate of a diol which is an addition compound of ethylene oxide or propylene oxide to hydrogenated bisphenol A, epoxy(meth)acrylate obtained by the addition of (meth)acrylate to diglycidyl ether of bisphenol A, diacrylate of polyoxyalkylene bisphenol A, and triethylene glycol divinyl ether.

Sources & evidence

ORD record
ord-7e4b0051a0ff4f59b1fb207b76cd4806
Source dataset
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06858657B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes