2-Naphthalenecarboxaldehyde → 3-(2-Naphthalenyl)-1-phenyl-2-propen-1-one
Reaction equation
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH:11]=O.[C:13]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)(=[O:15])[CH3:14]>>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH:11]=[CH:14][C:13]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[O:15]Participants
3
Procedure
By a procedure similar to that of example 1.59.1, starting from 2-naphthaldehyde and acetophenone, 3-(2-naphthalenyl)-1-phenylprop-2-en-1-one was obtained as yellowish solid.
Sources & evidence
- ORD record
- ord-ed0aad5db3314103b3c5d7abc540f393
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912186B2
Reaction notes
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