Isophthaloyl chloride → HCID 3090014, compound
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]=1Participants
4
Procedure
N,N'-Bis-(4-phenoxyphenyl)isophthalamide was prepared by the reaction of p-phenoxyaniline with isophthaloyl chloride. This amide (10.5117 g, 0.0210 moles) was polymerized with terephthaloyl chloride (4.3243 g, 0.0213 moles) by the procedure of Example 27. The cream colored fibrous polymer which was obtained had the repeat unit ##STR37##
Workup
- customThe cream colored fibrous polymer which was obtained
Sources & evidence
- ORD record
- ord-5d23a8cc5a0e4c24b30a5901eb1c4be2
- Source dataset
- uspto-grants-1995_07
- Patent number
- US05436310
Reaction notes
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