p-Anisoyl chloride → (4-methoxyphenyl)-(2-methyl-1-benzofuran-3-yl)methanone

HRID 1283650Notes

Reaction equation

HRID 1283650 reaction equation
[CH3:1][C:2]1[O:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[CH:6]=1.[C:11](Cl)(=[O:20])[C:12]1[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=1>>[CH3:1][C:2]1[O:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[C:6]=1[C:11](=[O:20])[C:12]1[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=1

Participants

3

Procedure

2-Methylbenzofuran (7.25 g., 0.055 mol.) was acylated with 15.7 g. (0.092 mol.) of anisoyl chloride according to the procedure described in Example 10 to give 2-methyl-3-(4'-methoxybenzoyl)benzofuran.

Sources & evidence

ORD record
ord-0eb5d53e983b42ef8e34c13f4a13e8f9
Source dataset
uspto-grants-1976_08
Patent number
US03975537

Reaction notes

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