p-Anisoyl chloride → HCID 10111601, compound

HRID 1743230Notes

Reaction equation

HRID 1743230 reaction equation
[CH3:1][C:2]1[O:3][C:4]2[C:16]([CH3:17])=[C:15]([CH3:18])[C:14]([OH:19])=[C:13]([CH3:20])[C:5]=2[C:6]=1[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[CH3:21][O:22][C:23]1[CH:31]=[CH:30][C:26]([C:27](Cl)=[O:28])=[CH:25][CH:24]=1>>[CH3:21][O:22][C:23]1[CH:31]=[CH:30][C:26]([C:27]([O:19][C:14]2[C:15]([CH3:18])=[C:16]([CH3:17])[C:4]3[O:3][C:2]([CH3:1])=[C:6]([C:7]4[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=4)[C:5]=3[C:13]=2[CH3:20])=[O:28])=[CH:25][CH:24]=1

Participants

3

Reactant 2

HCID 7477p-Anisoyl chlorideHCID 22238272HCID 22238272, compound

Product 1

HCID 10111601HCID 10111601, compoundYield 64%

Procedure

Using 2,4,6,7-tetramethyl-3-phenylbenzofuran-5-ol and 4-methoxybenzoyl chloride, the title compound was obtained in the same manner as in Example 26.

Sources & evidence

ORD record
ord-f0da4b38785c48f48183a95e159a78f6
Source dataset
uspto-grants-2006_03
Patent number
US07008950B1

Reaction notes

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