1-Acetylnaphthalene → HCID 53791153, compound
Reaction equation
C1([C:11](=[O:31])/[CH:12]=[CH:13]/[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[CH2:20][CH2:21][CH2:22][CH2:23][O:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)C2C(=CC=CC=2)C=CC=1.C(C1C2C(=CC=CC=2)C=CC=1)(=[O:34])C.O(C[CH2:53][CH2:54][CH2:55][C:56]1[CH:63]=[CH:62][CH:61]=[CH:60][C:57]=1[CH:58]=[O:59])C1C=CC=CC=1>>[O:24]([CH2:23][CH2:22][CH2:21][CH2:20][C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=1[C@@H:13]1[O:34][C@H:12]1[C:11]([O:59][C:58]1[C:57]2[C:56](=[CH:63][CH:62]=[CH:61][CH:60]=2)[CH:55]=[CH:54][CH:53]=1)=[O:31])[C:25]1[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1Participants
4
Procedure
Preparation of (E)-1-(1-naphthalenyl)-3-[2-(4-phenoxybutyl)phenyl]-2-propen-1-one. Using the method of Example 5a, 1'-acetonaphthone is reacted with 2-(4-phenoxybutyl)benzaldehyde in alcohol solution to give the titled compound.
Sources & evidence
- ORD record
- ord-b4561356c9dd4b51806d4ad7a612e180
- Source dataset
- uspto-grants-1992_05
- Patent number
- US05110959
Reaction notes
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