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HCID 22850137、化合物 → 133345-69-4

HRID 2210766
ノート
印刷プレビュー

反応式

HRID 2210766 の反応式
[NH2:1][CH2:2][C@H:3]([OH:13])[CH2:4][P:5]([CH3:12])(=[O:11])[O:6]CC(C)C>Cl>[NH2:1][CH2:2][C@H:3]([OH:13])[CH2:4][P:5]([CH3:12])(=[O:6])[OH:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 22850137HCID 22850137、化合物

生成物 1

HCID 5310933133345-69-4

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

A solution of 1.1 g of isobutyl P-[3-amino-2(S)-hydroxy-propyl]-P-methyl-phosphinate in 20 ml of 36% aqueous hydrochloric acid is heated to reflux for a period of 12 hours. The reaction mixture is then allowed to cool to room temperature, concentrated under reduced pressure, and co-evaporated four times with 25 ml of water. The crude material is dissolved in water, washed with ether and the aqueous layer is treated with activated charcoal. The solution is filtered hot, the filtrate is concentrated under reduced pressure, the residue dissolved in 20 ml of ethanol and treated with 1 ml of propylene oxide. The mixture is stirred until the precipitated solid is free of halogen. The solid is then filtered and recrystallised from methanol/acetone give P-[3-amino-2(S)-hydroxypropyl]-P- methyl-phosphinic acid, m.p. 221°-222.5°, 31P-NMR spectrum: δ=+38.9 ppm (D2O), [α]D25 =-6.0° (c=0.887% in H2O).

後処理

  1. temperatureto reflux for a period of 12 hours
  2. concentrationconcentrated under reduced pressure
  3. dissolutionThe crude material is dissolved in water
  4. washwashed with ether
  5. additionthe aqueous layer is treated with activated charcoal
  6. filtrationThe solution is filtered hot
  7. concentrationthe filtrate is concentrated under reduced pressure
  8. dissolutionthe residue dissolved in 20 ml of ethanol
  9. additiontreated with 1 ml of propylene oxide
  10. filtrationThe solid is then filtered
  11. customrecrystallised from methanol/acetone

出典と根拠

ORDレコード
ord-3986d76505b94334b430cdd882381a4b
出典データセット
uspto-grants-1995_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05461040

反応ノート

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