Water → Methyl alpha-Methyl-9-nitro-9,10-dihydroanthracene-10-acetate
反応式
[N+:1]([C:4]1[C:5]2[C:10]([CH:11]=[C:12]3[C:17]=1[CH:16]=[CH:15][CH:14]=[CH:13]3)=[CH:9][CH:8]=[CH:7][CH:6]=2)([O-:3])=[O:2].CN([S+](N(C)C)N(C)C)C.C[Si-](F)(F)(C)C.OP([O-])(O)=O.[K+].[OH2:40].[CH2:41]1[CH2:45][O:44][CH2:43][CH2:42]1>C(#N)C.CCOCC>[CH3:41][CH:42]([CH:11]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]([N+:1]([O-:3])=[O:2])[C:17]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]1=2)[C:43]([O:44][CH3:45])=[O:40]参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of 0.757 g (3.39 mmol) of 9-nitroanthracene and 0.663 mL (3.56 mmol) of MTS in 20 mL of anhydrous THF was added 0.941 g (3.42 mmol) of TASF in 2 mL of anhydrous acetonitrile at -78° C. The mixture was stirred for 24 hr. at -78° C. Then, ten mL of saturated KH2PO4 and 20 mL of water were added, the mixture was warmed to room temperature, and the product was extracted into ether. The combined ether extract was washed with water, dried, and concentrated. The major product, 0.491 g (56%), was isolated by column chromatography on silica using 20° ether/hexane as the solvent. Addition of small amount of ether to the major fraction yielded a light yellow solid. The product was analyzed by ultraviolet absorption, infrared spectroscopy, nuclear magnetic resonance spectroscopy, and mass spectrometry.
後処理
- customat -78° C
- extractionthe product was extracted into ether
- extractionThe combined ether extract
- washwas washed with water
- customdried
- concentrationconcentrated
- customThe major product, 0.491 g (56%), was isolated by column chromatography on silica using 20° ether/hexane as the solvent
- customyielded a light yellow solid
- customThe product was analyzed by ultraviolet absorption
出典と根拠
- ORDレコード
- ord-bd691a6101bf48498f40201522791a6d
- 出典データセット
- uspto-grants-1987_04
- 特許番号
- US04659862
反応ノート
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