反応式
[CH3:1][C:2]1([CH3:33])[CH2:11][CH2:10][C:9]([CH3:13])([CH3:12])[C:8]2[CH:7]=[C:6]([C:14]([O:16][C:17]3[CH:32]=[CH:31][C:20]([C:21]([O:23][CH2:24][C:25]4C=CC=CC=4)=[O:22])=[CH:19][CH:18]=3)=[O:15])[CH:5]=[CH:4][C:3]1=2.OC1C=CC(C(OCC2C=CC=CC=2)=O)=CC=1>>[CH3:33][C:2]1([CH3:1])[CH2:11][CH2:10][C:9]([CH3:12])([CH3:13])[C:8]2[CH:7]=[C:6]([C:14]([O:16][C:17]3[CH:18]=[CH:19][C:20]([C:21]([O:23][CH2:24][CH3:25])=[O:22])=[CH:31][CH:32]=3)=[O:15])[CH:5]=[CH:4][C:3]1=2参加物
3
実験手順
Benzyl 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoate-Using benzyl 4-hydroxybenzoate, the title compound was synthesized as a white, crystalline solid. PMR (CDCl3): δ 1.32 (6H, s), 1.35 (6H, s), 1.72 (4H, s), 5.38 (2H, s), 7.24-7.48 (8H, m), 7.92 (1H, dd, J~8.8 Hz, 1.8 Hz), 8.12-8.20 (3H, m).
出典と根拠
- ORDレコード
- ord-770a4a5b1b1741169dd4bb104aa007e7
- 出典データセット
- uspto-grants-1993_07
- 特許番号
- US05231113
関連ノート
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