p-Anisoyl chloride → HCID 68137439, compound

HRID 1658460Notes

Reaction equation

HRID 1658460 reaction equation
C1([C:7]2[O:11][C:10]([C:12]3[CH:20]=[CH:19][CH:18]=[CH:17][C:13]=3[C:14]([OH:16])=[O:15])=[N:9][N:8]=2)C=CC=CC=1.[C:21](Cl)(=O)[C:22]1[CH:27]=[CH:26][C:25]([O:28][CH3:29])=[CH:24][CH:23]=1>>[CH2:21]([C:7]1[O:11][C:10]([C:12]2[CH:20]=[CH:19][CH:18]=[CH:17][C:13]=2[C:14]([OH:16])=[O:15])=[N:9][N:8]=1)[C:22]1[CH:27]=[CH:26][C:25]([O:28][CH3:29])=[CH:24][CH:23]=1

Participants

3

Reactant 2

HCID 7477p-Anisoyl chlorideHCID 123920922-(5-Phenyl-1,3,4-oxadiazol-2-yl)benzoic acid

Product 1

HCID 68137439HCID 68137439, compound

Procedure

The same procedure is used as that for the preparation of 2-(5-phenyl-1,3,4-oxadiazole-2-yl) benzoic acid, Example 7, Method IIIb. The quantities of reagents used differ and p-anisoyl chloride was used in place of benzoyl chloride.

Sources & evidence

ORD record
ord-5ff88cdc60494c10a75d78fec6b76f31
Source dataset
uspto-grants-1976_06
Patent number
US03964896

Reaction notes

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