Hydrazine hydrate (1:1) → (S)-4-benzyloxy-3-hydroxybutanohydrazide

HRID 2186488ノート

反応式

HRID 2186488 の反応式
[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

4

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

  1. customIn a 100 ml flask were put
  2. temperaturethe mixture was heated
  3. temperatureunder reflux for 20 hours
  4. customwas removed by evaporation under reduced pressure
  5. additionTo the residue was added 40 ml of diethyl ether
  6. temperatureby heating
  7. temperatureunder reflux
  8. dissolutionto dissolve the crude crystals
  9. customThe crystals thus precipitated
  10. filtrationwere collected by filtration
  11. 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…