2-Acetylnaphthalene → HCID 66760010, compound
Reaction equation
[N: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.[CH:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15][C:14]=1[C:23](=[O:25])[CH3:24]>>[CH:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15][C:14]=1[C:23](=[O:25])[CH:24]=[CH:11][C:2]1[CH:3]=[CH:4][C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[N:1]=1Participants
3
Procedure
Synthesised according to example 1.59.1 using quinoline-2-carbaldehyde (3.0 g, 19.09 mmol) and 1-(naphthalen-2-yl)ethanone (3.25 g, 19.09 mmol); yellow solid; yield: 4.95 g (84%);
Workup
- customSynthesised
Sources & evidence
- ORD record
- ord-7a0d0f0eb7d440bbb57c9fcb8f7e6a63
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912186B2
Reaction notes
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