2,2-Diphenylpropionic acid → HCID 10298582, compound

HRID 2396284Notes

Reaction equation

HRID 2396284 reaction equation
CC(C1C=CC=C(C(C)C)C=1CC([C:16]1[C:17]([CH:30]([CH3:32])[CH3:31])=[C:18]([O:25][S:26](=[O:29])(=[O:28])[NH2:27])[C:19]([CH:22]([CH3:24])[CH3:23])=[CH:20][CH:21]=1)=O)C.C(C1C=CC=C(C(C)C)C=1CC(O)=O)(C)C.[C:49]1([C:55]([C:60]2[CH:65]=[CH:64][CH:63]=[CH:62][CH:61]=2)([CH3:59])[C:56](O)=[O:57])[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=1>>[O:57]=[C:56]([C:16]1[C:17]([CH:30]([CH3:31])[CH3:32])=[C:18]([O:25][S:26](=[O:29])(=[O:28])[NH2:27])[C:19]([CH:22]([CH3:23])[CH3:24])=[CH:20][CH:21]=1)[C:55]([C:49]1[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=1)([C:60]1[CH:65]=[CH:64][CH:63]=[CH:62][CH:61]=1)[CH3:59]

Participants

4

Procedure

This compound was prepared in the same manner as for the title compound of Example 1, except that 2,6-diisopropylphenylacetic acid was replaced with 2,2-diphenylpropionic acid, mp 140°-145° C.

Sources & evidence

ORD record
ord-191f1583016b4b3aba6cb51ef2d958c0
Source dataset
uspto-grants-1996_02
Patent number
US05491172

Reaction notes

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