Benzaldehyde → HCID 66759599, compound

HRID 1402955Notes

Reaction equation

[CH:1](=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:9]([C:12]1[CH:24]=[CH:23][C:22]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[NH:15][C:14]=2[CH:13]=1)(=[O:11])[CH3:10]>>[CH:13]1[C:14]2[NH:15][C:16]3[C:21](=[CH:20][CH:19]=[CH:18][CH:17]=3)[C:22]=2[CH:23]=[CH:24][C:12]=1[C:9](=[O:11])[CH:10]=[CH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

Reactant 2

HCID 240Benzaldehyde

HCID 2673322-Acetylcarbazole

Product 1

HCID 66759599HCID 66759599, compound

Procedure

By a procedure similar to that of example 1.59.1, starting from benzaldehyde and 2-acetylcarbazole, 1-(9H-carbazol-2-yl)-3-phenylprop-2-en-1-one was obtained as yellow solid.

Sources & evidence

ORD record: ord-d2e2fba97426406b8e5f833722b391fa
Source dataset: uspto-grants-2014_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08912186B2

Reaction notes

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