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Hydrochloric Acid → (2-Benzyloxycarbonylamino-ethyl)-phosphonic acid diethyl ester

HRID 1614910
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HRID 1614910 반응식
Cl.[CH2:2]([O:4][P:5]([CH2:10][CH2:11][NH2:12])(=[O:9])[O:6][CH2:7][CH3:8])[CH3:3].[C:13](Cl)([O:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:14].CCN(C(C)C)C(C)C>C(Cl)Cl.CCOC(C)=O>[CH2:7]([O:6][P:5]([CH2:10][CH2:11][NH:12][C:13]([O:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:14])(=[O:9])[O:4][CH2:2][CH3:3])[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 10387Benzyl chloroformateHCID 81531DiisopropylethylamineHCID 2733596Diethyl (2-aminoethyl)phosphonate

생성물 1

HCID 12487964(2-Benzyloxycarbonylamino-ethyl)-phosphonic acid diethyl ester

시약·촉매·용매 2

HCID 6344Dichloromethane용매
HCID 8857Ethyl Acetate용매

실험 절차

The HCl salt of (2-amino-ethyl)-phosphonic acid diethyl ester (4.5 g, 20.7 mmol) was dissolved in CH2Cl2 (100 mL). To this solution was added CBzCl (3.2 mL, 22.7 mmol), followed by iPr2NEt (14.4 mL, 82.8 mmol). The reaction was stirred at room temperature until complete, as determined by TLC (eluent: 100% EtOAc). The reaction was quenched by the addition of saturated NaHCO3. The mixture was then partitioned between CH2Cl2 and H2O. The layers were separated and the organic layer was washed with brine and then dried over Na2SO4. The drying agent was removed by vacuum filtration and (2-benzyloxycarbonylamino-ethyl)-phosphonic acid diethyl ester was isolated from the concentrated filtrate by silica gel column chromatography (EtOAc/hexanes) (5.98 g, 92%).

후처리

  1. customThe reaction was quenched by the addition of saturated NaHCO3
  2. customThe mixture was then partitioned between CH2Cl2 and H2O
  3. customThe layers were separated
  4. washthe organic layer was washed with brine
  5. dry with materialdried over Na2SO4
  6. customThe drying agent was removed by vacuum filtration

출처 및 근거

ORD 기록
ord-b1d439d00c2d435ab18937b37453f277
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08765722B2

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