m-Anisoyl chloride → HCID 15481277, compound

HRID 1873126Notes

Reaction equation

HRID 1873126 reaction equation
[CH2:1]([C:8]1[S:12][C:11]2[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=2[CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:17](Cl)(=[O:26])[C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([O:24][CH3:25])[CH:19]=1>>[CH2:1]([C:8]1[S:12][C:11]2[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=2[C:9]=1[C:17]([C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([O:24][CH3:25])[CH:19]=1)=[O:26])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 74374m-Anisoyl chlorideHCID 127581572-Benzyl-1-benzothiophene

Product 1

HCID 15481277HCID 15481277, compound

Procedure

Prepared from 2-benzyl-benzo[b]thiophene and m-anisoyl chloride according to the procedure in Example 8. White solid: MS (EI): [M+], 358.

Sources & evidence

ORD record
ord-1c0c366310374ff2b0539582c55364f3
Source dataset
uspto-grants-2000_08
Patent number
US06110962

Reaction notes

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