4-Chlorobenzoyl chloride → 2-p-Chlorobenzoyl-3-p-methoxyphenylbenzofuran

HRID 1414634Notes

Reaction equation

HRID 1414634 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=3[O:11][CH:10]=2)=[CH:5][CH:4]=1.[Cl:18][C:19]1[CH:27]=[CH:26][C:22]([C:23](Cl)=[O:24])=[CH:21][CH:20]=1>>[Cl:18][C:19]1[CH:27]=[CH:26][C:22]([C:23]([C:10]2[O:11][C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=3[C:9]=2[C:6]2[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)=[O:24])=[CH:21][CH:20]=1

Participants

3

Reactant 2

HCID 85014-Chlorobenzoyl chlorideHCID 121700553-p-Methoxyphenylbenzofuran

Product 1

HCID 107137122-p-Chlorobenzoyl-3-p-methoxyphenylbenzofuran

Procedure

When 3-p-methoxyphenylbenzofuran was acylated with p-chlorobenzoyl chloride as described in the procedure of Example 1, 2-p-chlorobenzoyl-3-p-methoxyphenylbenzofuran was obtained.

Sources & evidence

ORD record
ord-a44071d5042748a4b7194b0af82e7361
Source dataset
uspto-grants-1977_01
Patent number
US04001426

Reaction notes

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