3',4',5'-Trifluoroacetophenone → HCID 57830662、化合物
反応式
B(Cl)([C@@H]1[C@@H](C)[C@@H]2C(C)(C)[C@@H](C2)C1)[C@@H]1[C@@H](C)[C@@H]2C(C)(C)[C@@H](C2)C1.[CH3:23][C:24]([C:26]1[CH:31]=[C:30]([F:32])[C:29]([F:33])=[C:28]([F:34])[CH:27]=1)=[O:25]>C1COCC1>[F:32][C:30]1[CH:31]=[C:26]([C@H:24]([OH:25])[CH3:23])[CH:27]=[C:28]([F:34])[C:29]=1[F:33]参加物
実験手順
To a solution of (+)-DIP-chloride (11.8 g) in THF (200 ml) cooled to −30° C., 3,4,5-trifluoroacetophenone (5.0 g) [CAS 220141-73-1] was added dropwise in a nitrogen atmosphere. The reaction solution was stirred at the same temperature for five hours and at room temperature at one hour, and then THF was evaporated under reduced pressure. 6.5 ml of diethanolamine was added dropwise to a solution of the resulting residue in diethyl ether (150 ml), and the reaction solution was stirred at room temperature overnight. The insoluble matter was removed by filtration, and then the solvent was evaporated. Hexane was added to the resulting residue, and the insoluble matter was removed by filtration again. The filtrate was purified by silica gel column chromatography (heptane:ethyl acetate=19:1 to 4:1) to obtain 3.69 g of the title compound.
後処理
- customTHF was evaporated under reduced pressure
- addition6.5 ml of diethanolamine was added dropwise to a solution of the resulting residue in diethyl ether (150 ml)
- stirringthe reaction solution was stirred at room temperature overnight
- customThe insoluble matter was removed by filtration
- customthe solvent was evaporated
- additionHexane was added to the resulting residue
- customthe insoluble matter was removed by filtration again
- customThe filtrate was purified by silica gel column chromatography (heptane:ethyl acetate=19:1 to 4:1)
出典と根拠
- ORDレコード
- ord-65d8b3469c5543729eaba1811b9c0dea
- 出典データセット
- uspto-grants-2009_11
- 特許番号
- US07618960B2
反応ノート
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