Acetophenone → HCID 3114295, compound

HRID 1402912Notes

Reaction equation

HRID 1402912 reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH:10]=O)=[CH:2]1.[C:12]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)(=[O:14])[CH3:13]>>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH:10]=[CH:13][C:12]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[O:14])=[CH:2]1

Participants

3

Reactant 2

HCID 7410AcetophenoneHCID 10256Indole-3-Carboxaldehyde

Product 1

HCID 3114295HCID 3114295, compound

Procedure

By a procedure similar to that of example 1.59.1, starting from commercial 3-indolecarbaldehyde and acetophenone, 3-(1H-indol-3-yl)-1-phenylprop-2-en-1-one was obtained as yellow solid.

Sources & evidence

ORD record
ord-4dd7c7163c7c482ca31b58a120a9bf97
Source dataset
uspto-grants-2014_12
Patent number
US08912186B2

Reaction notes

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