Benzoyl chloride → HCID 15406406, compound

HRID 1415687Notes

Reaction equation

HRID 1415687 reaction equation
[C:1]1([C:7]2[C:8]3[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][C:9]=3[S:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:18](Cl)(=[O:25])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[C:18]([C:11]1[S:10][C:9]2[CH:12]=[C:13]([O:16][CH3:17])[CH:14]=[CH:15][C:8]=2[C:7]=1[C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)(=[O:25])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1

Participants

3

Reactant 2

HCID 7412Benzoyl chlorideHCID 15422638HCID 15422638, compound

Product 1

HCID 15406406HCID 15406406, compoundYield 52%

Procedure

3-Phenyl-6-methoxybenzo[b]thiophene and benzoyl chloride were converted to the title compound by the procedure of Example 1 in 52% yield, after crystallization from methanol.

Sources & evidence

ORD record
ord-c66ae3f200e94686b622c0360619cc01
Source dataset
uspto-grants-1999_06
Patent number
US05908859

Reaction notes

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