p-Anisoyl chloride → HCID 21435366, compound

HRID 2398487Notes

Reaction equation

HRID 2398487 reaction equation
C(C1OC2C=CC(Br)=CC=2C=1)C1C=CC=CC=1.C(Cl)(=O)C1C=CC(OC)=CC=1.[CH2:29]([C:36]1[O:37][C:38]2[CH:54]=[CH:53][C:52]([Br:55])=[CH:51][C:39]=2[C:40]=1[C:41](=[O:50])[C:42]1[CH:47]=[CH:46][C:45]([O:48][CH3:49])=[CH:44][CH:43]=1)[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1.[CH2:56]([N:58]([CH2:63][CH3:64])[CH2:59][CH2:60]CCl)[CH3:57]>>[CH2:29]([C:36]1[O:37][C:38]2[CH:54]=[CH:53][C:52]([Br:55])=[CH:51][C:39]=2[C:40]=1[C:41](=[O:50])[C:42]1[CH:47]=[CH:46][C:45]([O:48][CH2:49][CH2:57][CH2:56][N:58]([CH2:63][CH3:64])[CH2:59][CH3:60])=[CH:44][CH:43]=1)[C:30]1[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=1

Participants

5

Reactant 4

HCID 7477p-Anisoyl chlorideHCID 669183-Chloropropyl(diethyl)amineHCID 21435285HCID 21435285, compoundHCID 227689092-Benzyl-5-bromo-1-benzofuran

Product 1

HCID 21435366HCID 21435366, compound

Procedure

2-Benzyl-5-bromobenzofuran is acylated with p-anisoyl chloride as described above and the resulting 2-benzyl-5-bromo-3-(4-methoxybenzoyl)benzofuran is demethylated and the product reacted with 3-diethylaminopropyl chloride as previously described to give the title compound.

Sources & evidence

ORD record
ord-346dc76786674c77b9fd5532174262a5
Source dataset
uspto-grants-1977_05
Patent number
US04024273

Reaction notes

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