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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 22850137, 화합물 → 133345-69-4

HRID 865839
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HRID 865839 반응식
[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]
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참가 물질

3

반응물 1

HCID 22850137HCID 22850137, 화합물

생성물 1

HCID 5310933133345-69-4

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

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)-hydroxy-propyl]-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).

후처리

  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

출처 및 근거

ORD 기록
ord-7e282b555fee4820bad9e47b503e055e
출처 데이터셋
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05567840

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