4,4'-Dichlorobenzophenone → HCID 15597559, compound

HRID 1494624Notes

Reaction equation

Cl[C:2]1[CH:16]=[CH:15][C:5]([C:6]([C:8]2[CH:13]=[CH:12][C:11](Cl)=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1.[NH2:17][C:18]1[CH:19]=[C:20]([OH:24])[CH:21]=[CH:22][CH:23]=1>>[NH2:17][C:18]1[CH:19]=[C:20]([CH:21]=[CH:22][CH:23]=1)[O:24][C:2]1[CH:16]=[CH:15][C:5]([C:6]([C:8]2[CH:13]=[CH:12][C:11]([O:24][C:20]3[CH:21]=[CH:22][CH:23]=[C:18]([NH2:17])[CH:19]=3)=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1

Participants

Reactant 2

HCID 70344,4'-Dichlorobenzophenone

HCID 115683-Aminophenol

Product 1

HCID 15597559HCID 15597559, compound

Procedure

4,4'-bis(m-aminophenoxy)benzophenone was prepared in accordance with the method of Example 1 employing 4,4'-dichlorobenzophenone and m-aminophenol as the starting materials. 26% yield of product having a melting point of about 138°-140° C. was obtained.

Sources & evidence

ORD record: ord-827cc1ee49054ffc95b958c8f4604150
Source dataset: uspto-grants-1991_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05026872

Reaction notes

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