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Acetic Anhydride → HCID 19805000, 화합물

HRID 1682311
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HRID 1682311 반응식
C(=O)([O-])O.[Na+].[C:6](OC(=O)C)(=[O:8])[CH3:7].[NH2:13][CH:14](/[CH:18]=[CH:19]/[CH2:20][P:21]([OH:24])([OH:23])=[O:22])[C:15]([OH:17])=[O:16]>O1CCOCC1.O>[NH:13]([CH:14](/[CH:18]=[CH:19]/[CH2:20][P:21]([OH:24])([OH:23])=[O:22])[C:15]([OH:17])=[O:16])[C:6]([CH3:7])=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7918Acetic AnhydrideHCID 516892Sodium BicarbonateHCID 6506250HCID 6506250, 화합물

생성물 1

HCID 19805000HCID 19805000, 화합물

시약·촉매·용매 1

HCID 218864351,4-Dioxane--water (1/1)용매

실험 절차

At 0°, 170 mg of sodium hydrogen carbonate and, within a period of 5 minutes, 50 microliters of acetic anhydride are added to a solution of 100 mg of E-2-amino-5-phosphono-3-pentenoic acid in 6 ml of dioxan/water (1:1). The whole is stirred for 30 minutes at 0°, approximately 2 ml of Dowex 50 H+ are added and filtration is carried out. The filtrate is concentrated by evaporation and purified by ion exchange chromatography (Dowex 50 H+). Lyophilisation of the pure fractions yields 110 mg of E-2-acetamino-5-phosphono-3-pentenoic acid, m.p. 155°.

후처리

  1. additionapproximately 2 ml of Dowex 50 H+ are added
  2. filtrationfiltration
  3. concentrationThe filtrate is concentrated by evaporation
  4. custompurified by ion exchange chromatography (Dowex 50 H+)

출처 및 근거

ORD 기록
ord-e80af50fdefa47898159bed0127fba29
출처 데이터셋
uspto-grants-1992_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05175344

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