p-Anisoyl chloride → HCID 21488060, compound

HRID 1414635Notes

Reaction equation

HRID 1414635 reaction equation
[C:1](Cl)(=[O:10])[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][CH:3]=1.[Br:12][CH2:13][CH2:14][O:15][C:16]1[CH:21]=[CH:20][C:19]([C:22]2[O:23][C:24]3[CH:30]=[CH:29][CH:28]=[CH:27][C:25]=3[CH:26]=2)=[CH:18][CH:17]=1>>[Br:12][CH2:13][CH2:14][O:15][C:16]1[CH:21]=[CH:20][C:19]([C:22]2[O:23][C:24]3[CH:30]=[CH:29][CH:28]=[CH:27][C:25]=3[C:26]=2[C:1](=[O:10])[C:2]2[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][CH:3]=2)=[CH:18][CH:17]=1

Participants

3

Reactant 2

HCID 7477p-Anisoyl chlorideHCID 21487980HCID 21487980, compound

Product 1

HCID 21488060HCID 21488060, compound

Procedure

When p-anisoyl chloride and 2-[4'-(2-bromoethoxy)phenyl]benzofuran are reacted by the procedure described in Example 11 and the 2-[4'-(2-bromoethoxy)phenyl]-3-p-anisoylbenzofuran thus obtained is treated with piperidine as described in Example 11, the title compound is obtained.

Sources & evidence

ORD record
ord-4266760fb1474e24891e0a65ac9ad225
Source dataset
uspto-grants-1977_01
Patent number
US04001426

Reaction notes

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