Bisphenol A → HCID 86756476, compound

HRID 636793Notes

Reaction equation

[C:1]([Cl:12])(=[O:11])[C:2]1[CH:10]=[CH:9][C:5]([C:6]([Cl:8])=[O:7])=[CH:4][CH:3]=1.[OH:13][C:14]1[CH:19]=[CH:18][C:17]([C:20]([C:23]2[CH:28]=[CH:27][C:26]([OH:29])=[CH:25][CH:24]=2)([CH3:22])[CH3:21])=[CH:16][CH:15]=1>>[OH:13][C:14]1[CH:15]=[CH:16][C:17]([C:20]([C:23]2[CH:24]=[CH:25][C:26]([OH:29])=[CH:27][CH:28]=2)([CH3:22])[CH3:21])=[CH:18][CH:19]=1.[C:6]([Cl:8])(=[O:7])[C:5]1[CH:9]=[CH:10][C:2]([C:1]([Cl:12])=[O:11])=[CH:3][CH:4]=1

Participants

Reactant 2

HCID 6623Bisphenol A

HCID 7488Terephthaloyl chloride3×

Product 1

HCID 86756476HCID 86756476, compound

Procedure

Next, the terephthaloyl chloride vapor in the condensing chamber 2 was adiabatically expanded, and the introduced base particles were exposed thereto for 2 minutes. Consequently, terephthaloyl chloride condensed on the surface of the base particles. A polymerization reaction took place between terephthaloyl chloride condensed on the surface of the base particles and bisphenol A of the base particles, forming a film of bisphenol A—terephthaloyl chloride co-polymer on the surface of the base particles.

Workup

customA polymerization reaction

Sources & evidence

ORD record: ord-fcd59e67487242aeb76dfad7b54b7db9
Source dataset: uspto-grants-2001_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06194487B1

Reaction notes

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