反応式
[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:3])[CH3:2].[F:14][C:15]([F:25])([F:24])[C:16]([F:23])([F:22])[C:17](OCC)=[O:18]>>[F:22][C:16]([F:23])([C:15]([F:25])([F:24])[F:14])[C:17](=[O:18])[CH2:2][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:3]参加物
3
実験手順
The compound was synthesized according to example 1 using 2-acetylnaphthalene and ethyl pentafluoropropionate as starting materials. The product was crystallized from petroleum ether. 1H NMR (CDCl3): 6.79 (s, 1 H); 7.57-7.67 (m, 2H); 7.90 (bd, 1 H); 7.94-7.95 (m, 2H); 7.99 (bd, 1H); 8.53 (s, 1 H). IR (film): 1602 (C═O); 1201 (C—F).
後処理
- customThe compound was synthesized
- customThe product was crystallized from petroleum ether
出典と根拠
- ORDレコード
- ord-38bd0544e87d4ca6b596713afa8114c1
- 出典データセット
- uspto-grants-2008_06
- 特許番号
- US07381567B2
関連ノート
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