3,5-Dimethylbenzoyl Chloride → HCID 21488027, compound

HRID 1414639Notes

Reaction equation

HRID 1414639 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[S:10][C:11]3[CH:17]=[CH:16][CH:15]=[CH:14][C:12]=3[CH:13]=2)=[CH:5][CH:4]=1.[CH3:18][C:19]1[CH:20]=[C:21]([CH:25]=[C:26]([CH3:28])[CH:27]=1)[C:22](Cl)=[O:23]>>[CH3:18][C:19]1[CH:20]=[C:21]([CH:25]=[C:26]([CH3:28])[CH:27]=1)[C:22]([C:13]1[C:12]2[CH:14]=[CH:15][CH:16]=[CH:17][C:11]=2[S:10][C:9]=1[C:6]1[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1)=[O:23]

Participants

3

Reactant 2

HCID 810883,5-Dimethylbenzoyl ChlorideHCID 41373912-(4-Methoxyphenyl)benzothiophene

Product 1

HCID 21488027HCID 21488027, compound

Procedure

When 2-p-methoxyphenylbenzothiophene was acylated with 3,5-dimethylbenzoyl chloride as described in the procedure of Example 1, 3-(3',5'-dimethylbenzoyl)-2-(4'-methoxyphenyl)benzothiophene was obtained.

Sources & evidence

ORD record
ord-256fbe2cbba64e75b56c436c356a04cf
Source dataset
uspto-grants-1977_01
Patent number
US04001426

Reaction notes

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