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Styrene → Styrene glycidyl Methacrylate

HRID 48139
Notes
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Reaction equation

HRID 48139 reaction equation
[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:9]([O:14][CH2:15][CH:16]1[O:18][CH2:17]1)(=[O:13])[C:10]([CH3:12])=[CH2:11].C(C1C=CC=CC=1C=C)=C.C(OCC1OC1)(=O)C(C)=C.C(C1C=CC=CC=1C=C)=C>O>[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:9]([O:14][CH2:15][CH:16]1[O:18][CH2:17]1)(=[O:13])[C:10]([CH3:12])=[CH2:11]
ParticipantsProcedureSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 7501StyreneHCID 7837Glycidyl methacrylateHCID 666661,2-DiethenylbenzeneHCID 87578082Gma dvb

Product 1

HCID 21867792Styrene glycidyl Methacrylate

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

Styrene (St; Wako Pure Chemicals. It was used after distillation under reduced pressure of 21.5 mmHg at 46° C.), glycidyl methacrylate (GMA; Wako Pure Chemicals. It was used after distillation under reduced pressure of 2 mmHg at 33° C.), divinyl-benzene (DVB; Tokyo Kasei), 2,2′-azobis (2-amidinopropane dihydrochloride) (V-50; Wako Pure Chemicals) and water were used in the following compositional formula: St/GMA/DVB/V-50/H20=1.2/1.8+0.3/0.04/0.06/110 (g)

Sources & evidence

ORD record
ord-1040e15fbbf246af81fada7285e58ba9
Source dataset
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06703207B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes