HCID 19378570, compound → HCID 19378646, compound

HRID 2210469Notes

Reaction equation

HRID 2210469 reaction equation
CNS(C1C=C(C(=O)CC(CC2C=CC=CC=2)C(O)=O)C=CC=1)(=O)=O.[O:26]=[C:27]([C:40]1O[CH:42]=[C:43]2[CH:48]=[CH:47][CH:46]=C[C:44]=12)[CH2:28][CH:29]([CH2:33][C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)[C:30]([OH:32])=[O:31]>>[CH3:42][C:43]1[CH:44]=[C:40]([C:27](=[O:26])[CH2:28][CH:29]([CH2:33][C:34]2[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=2)[C:30]([OH:32])=[O:31])[CH:46]=[CH:47][CH:48]=1

Participants

3

Reactant 2

HCID 19378570HCID 19378570, compoundHCID 57261671HCID 57261671, compound

Product 1

HCID 19378646HCID 19378646, compound

Procedure

3-(methylaminosulfonyl)gamma-oxo-α-(phenylmethyl)benzenebutanoic acid, mp. 130°-133° C. gamma-oxo-alpha-(phenylmethyl)-2-benzofuranbutanoic acid, mp. 158°-161° C.

Sources & evidence

ORD record
ord-9ce6c9570e894522814126420fd94e4f
Source dataset
uspto-grants-1995_10
Patent number
US05459131

Reaction notes

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