p-Anisoyl chloride → 2-(4-Chlorophenyl)-3-(4-hydroxybenzoyl)benzofuran

HRID 1577021Notes

Reaction equation

HRID 1577021 reaction equation
ClC1C=CC(C2OC3C=CC=CC=3C=2)=CC=1.C(Cl)(=O)C1C=CC(OC)=CC=1.[Cl:28][C:29]1[CH:34]=[CH:33][C:32]([C:35]2[O:36][C:37]3[CH:53]=[CH:52][CH:51]=[CH:50][C:38]=3[C:39]=2[C:40](=[O:49])[C:41]2[CH:46]=[CH:45][C:44]([O:47]C)=[CH:43][CH:42]=2)=[CH:31][CH:30]=1.Cl.N1C=CC=CC=1>>[Cl:28][C:29]1[CH:34]=[CH:33][C:32]([C:35]2[O:36][C:37]3[CH:53]=[CH:52][CH:51]=[CH:50][C:38]=3[C:39]=2[C:40](=[O:49])[C:41]2[CH:46]=[CH:45][C:44]([OH:47])=[CH:43][CH:42]=2)=[CH:31][CH:30]=1

Participants

5

Reactant 4

HCID 7477p-Anisoyl chlorideHCID 43683122-(4-Chlorophenyl)-1-benzofuranHCID 10176127Pyridinium chlorideHCID 214352602-(4-Chlorophenyl)-3-(4-methoxybenzoyl)benzofuran

Product 1

HCID 214352692-(4-Chlorophenyl)-3-(4-hydroxybenzoyl)benzofuran

Procedure

When 2-(4-chlorophenyl)benzofuran was acylated with p-anisoyl chloride as described in the procedure of Example 1 and the resulting 2-(4-chlorophenyl)-3-(4-methoxybenzoyl)benzofuran was demethylated with pyridine hydrochloride as previously described, 2-(4-chlorophenyl)-3-(4-hydroxybenzoyl)benzofuran was obtained.

Sources & evidence

ORD record
ord-58b2c3ecba1c48bba9ceb0143e427104
Source dataset
uspto-grants-1976_09
Patent number
US03983245

Reaction notes

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