Bisphenol A diglycidyl ether → HCID 20510556, compound

HRID 1758196Notes

Reaction equation

HRID 1758196 reaction equation
[CH3:1][C:2]1([CH3:10])[CH2:7][CH2:6][CH2:5][C:4]([CH3:9])([CH3:8])[NH:3]1.[O:11]1[CH2:35][CH:12]1[CH2:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([C:21]([C:24]2[CH:29]=[CH:28][C:27]([O:30][CH2:31][CH:32]3[O:34][CH2:33]3)=[CH:26][CH:25]=2)([CH3:23])[CH3:22])=[CH:17][CH:16]=1>C(O)(C)(C)C>[OH:34][CH:32]([CH2:33][N:3]1[C:4]([CH3:9])([CH3:8])[CH2:5][CH2:6][CH2:7][C:2]1([CH3:10])[CH3:1])[CH2:31][O:30][C:27]1[CH:26]=[CH:25][C:24]([C:21]([C:18]2[CH:19]=[CH:20][C:15]([O:14][CH2:13][CH:12]([OH:11])[CH2:35][N:3]3[C:4]([CH3:9])([CH3:8])[CH2:5][CH2:6][CH2:7][C:2]3([CH3:10])[CH3:1])=[CH:16][CH:17]=2)([CH3:22])[CH3:23])=[CH:29][CH:28]=1

Participants

4

Reactant 2

HCID 2286Bisphenol A diglycidyl etherHCID 130352,2,6,6-Tetramethylpiperidine

Product 1

HCID 20510556HCID 20510556, compound

Reagents, catalysts & solvents 1

HCID 6386tert-ButanolSolvent

Procedure

To 50 ml of t-butanol were added 14.1 g of 2,2,6,6-tetramethylpiperidine and 10.2 g of 2,2-bis[p-(2,3-epoxypropoxy)phenyl]propane, and the mixture was reacted following the procedure described in Example 21 to give the desired Compound No. 1 in the form of white crystals melting at 110°-112° C.

Workup

  1. customthe mixture was reacted

Sources & evidence

ORD record
ord-19fd47614e6c43b1a2fd67715554bfa3
Source dataset
uspto-grants-1983_02
Patent number
US04371644

Reaction notes

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