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Hydrochloric Acid → (3-Amino-1-methyl-propyl)-methyl-phosphinic acid

HRID 2210763
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HRID 2210763 반응식
Cl.[NH2:2][CH2:3][CH2:4][CH:5]([P:7]([CH3:14])(=[O:13])[O:8]CC(C)C)[CH3:6]>>[NH2:2][CH2:3][CH2:4][CH:5]([P:7]([CH3:14])(=[O:8])[OH:13])[CH3:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 313Hydrochloric AcidHCID 23374771isobutyl P-(4-aminobut-2-yl)-P-methyl-phosphinate

생성물 1

HCID 10219532(3-Amino-1-methyl-propyl)-methyl-phosphinic acid

실험 절차

A solution of 21.5 g of isobutyl P-(4-aminobut-2-yl)-P-methyl-phosphinate 80 ml of 36% aqueous hydrochloric acid is heated to reflux for a period of 10 hours. The reaction mixture is then allowed to cool to room temperature, concentrated under reduced pressure, and co-evaporated twice with 100 ml of water. The crude material is dissolved in water, washed with chloroform, and the aqueous layer treated with activated charcoal. The aqueous solution is filtered hot, evaporated to dryness, the crude product is dissolved in 50 ml of methanol and treated with 1-2 ml of propylene oxide. The hygroscopic solid is filtered and triturated with acetone. After drying, P-(4-aminobut-2-yl)-P-methyl-phosphinic acid is obtained as a hygroscopic solid, m.p. 68°-75°, 31P-NMR spectrum: δ=+46.5 ppm (D2O).

후처리

  1. temperature
to reflux for a period of 10 hours
  • concentrationconcentrated under reduced pressure
  • dissolutionThe crude material is dissolved in water
  • washwashed with chloroform
  • additionthe aqueous layer treated with activated charcoal
  • filtrationThe aqueous solution is filtered hot
  • customevaporated to dryness
  • dissolutionthe crude product is dissolved in 50 ml of methanol
  • additiontreated with 1-2 ml of propylene oxide
  • filtrationThe hygroscopic solid is filtered
  • customtriturated with acetone
  • customAfter drying
  • 출처 및 근거

    ORD 기록
    ord-3f58d52094ef4b53a48c46d77406a435
    출처 데이터셋
    uspto-grants-1995_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05461040

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