Hydrazine hydrate (1:1) → (S)-4-benzyloxy-3-hydroxybutanohydrazide
反応式
[CH2:1]([O:8][CH2:9][C@@H:10]([OH:17])[CH2:11][C:12](OCC)=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O.[NH2:19][NH2:20]>C(O)C>[CH2:1]([O:8][CH2:9][C@@H:10]([OH:17])[CH2:11][C:12]([NH:19][NH2:20])=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
反応条件
- 温度
- 5 °C
実験手順
In a 100 ml flask were put 4.15 g (17.4 mmol) of ethyl (S)-4-benzyloxy-3-hydroxybutyrate (optical purity: 89%e.e.) prepared in Reference Example 2, 20 ml of ethanol, and 2.62 g (52.2 mmol) of hydrazine monohydrate in a nitrogen stream, and the mixture was heated under reflux for 20 hours. The reaction mixture was cooled to room temperature (22 to 24° C.), and ethanol was removed by evaporation under reduced pressure. To the residue was added 40 ml of diethyl ether, followed by heating under reflux to dissolve the crude crystals. The solution was cooled to 5° C., followed by stirring for 1 hour. The crystals thus precipitated were collected by filtration and washed with 10 ml of diethyl ether to give 2.90 g (74%) of the title compound. Melting point: 96.9° C. Optical purity: >99.9%e.e.
後処理
- customIn a 100 ml flask were put
- temperaturethe mixture was heated
- temperatureunder reflux for 20 hours
- customwas removed by evaporation under reduced pressure
- additionTo the residue was added 40 ml of diethyl ether
- temperatureby heating
- temperatureunder reflux
- dissolutionto dissolve the crude crystals
- customThe crystals thus precipitated
- filtrationwere collected by filtration
- washwashed with 10 ml of diethyl ether
出典と根拠
- ORDレコード
- ord-91bf0004919c40f0b1647304f7844eda
- 出典データセット
- uspto-grants-2002_06
- 特許番号
- US06403804B1
反応ノート
読み込み中…