2-Acetylnaphthalene → HCID 53676670, compound

HRID 1402908Notes

Reaction equation

HRID 1402908 reaction equation
[C:1]([C:4]1[CH:13]=[CH:12][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=1)(=O)[CH3:2].[Cl:14][C:15]1[CH:22]=[CH:21][C:18]([CH:19]=[O:20])=[CH:17][CH:16]=1>>[Cl:14][C:15]1[CH:22]=[CH:21][C:18]([C:19](=[O:20])[CH:2]=[CH:1][C:4]2[CH:13]=[CH:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[CH:5]=2)=[CH:17][CH:16]=1

Participants

3

Reactant 2

HCID 71222-AcetylnaphthaleneHCID 77264-Chlorobenzaldehyde

Product 1

HCID 53676670HCID 53676670, compound

Procedure

By a procedure similar to that of example 1.59.1, starting from commercial 2-acetylnaphthalene and 4-chlorobenzaldehyde, 1-(4-chlorophenyl)-3-(2-naphthalenyl)prop-2-en-1-one was obtained as yellowish solid.

Sources & evidence

ORD record
ord-70c57b4f7460458b8bf2a92e0381a52e
Source dataset
uspto-grants-2014_12
Patent number
US08912186B2

Reaction notes

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