1-Phenylcyclopentanecarboxylic acid → HCID 10224572, compound

HRID 2396281Notes

Reaction equation

HRID 2396281 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]2([C:60]([OH:62])=O)[CH2:59][CH2:58][CH2:57][CH2:56]2)[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=1>>[C:49]1([C:55]2([C:60]([C:16]3[C:17]([CH:30]([CH3:32])[CH3:31])=[C:18]([O:25][S:26](=[O:28])(=[O:29])[NH2:27])[C:19]([CH:22]([CH3:24])[CH3:23])=[CH:20][CH:21]=3)=[O:62])[CH2:56][CH2:57][CH2:58][CH2:59]2)[CH:50]=[CH:51][CH:52]=[CH:53][CH:54]=1

Participants

4

Reactant 3

HCID 661671-Phenylcyclopentanecarboxylic acidHCID 10226443Sulfamic acid[[2,6-bis(1-methylethyl)phenyl]-acetyl]-2,6-bis(1-methylethyl)phenyl esterHCID 152779902-(2,6-Diisopropylphenyl)acetic acid

Product 1

HCID 10224572HCID 10224572, compound

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 1-phenyl-1-cyclopentanecarboxylic acid, mp 149°-152° C.

Sources & evidence

ORD record
ord-c3c8a8e2670c4d0aac5672809db36537
Source dataset
uspto-grants-1996_02
Patent number
US05491172

Reaction notes

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