Isophthaloyl chloride → HCID 3090014, compound

HRID 1608088Notes

Reaction equation

HRID 1608088 reaction equation
[O:1]([C:8]1[CH:14]=[CH:13][C:11]([NH2:12])=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:15](Cl)(=[O:25])[C:16]1[CH:24]=[CH:23][CH:22]=[C:18]([C:19](Cl)=[O:20])[CH:17]=1.C(Cl)(=O)[C:28]1[CH:36]=[CH:35][C:31](C(Cl)=O)=[CH:30][CH:29]=1>>[O:1]([C:8]1[CH:9]=[CH:10][C:11]([NH:12][C:15](=[O:25])[C:16]2[CH:24]=[CH:23][CH:22]=[C:18]([C:19]([NH:12][C:11]3[CH:13]=[CH:14][C:8]([O:1][C:28]4[CH:29]=[CH:30][CH:31]=[CH:35][CH:36]=4)=[CH:9][CH:10]=3)=[O:20])[CH:17]=2)=[CH:13][CH:14]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Procedure

N,N'-Bis-(4-phenoxyphenyl)isophthalamide was prepared by the reaction of p-phenoxyaniline with isophthaloyl chloride. This amide (10.5117 g, 0.0210moles) was polymerized with terephthaloyl chloride (4.3243 g, 0.0213 moles)by the procedure of Example 27. The cream colored fibrous polymer which wasobtained had the repeat unit ##STR37##

Sources & evidence

ORD record
ord-371ceb5522894f06a1e02ec58e068a7a
Source dataset
uspto-grants-1989_09
Patent number
US04868271

Reaction notes

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