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Benzoyl chloride → Methyl 2-benzamido-2-(dimethoxyphosphoryl)acetate

HRID 322933
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반응식

HRID 322933 반응식
[NH2:1][CH:2]([P:7]([O:11][CH3:12])([O:9][CH3:10])=[O:8])[C:3]([O:5][CH3:6])=[O:4].[C:13](Cl)(=[O:20])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>ClCCl>[C:13]([NH:1][CH:2]([P:7]([O:11][CH3:12])([O:9][CH3:10])=[O:8])[C:3]([O:5][CH3:6])=[O:4])(=[O:20])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7412Benzoyl chlorideHCID 11084793Methyl 2-amino-2-(dimethoxyphosphoryl)acetate

생성물 1

HCID 14104867Methyl 2-benzamido-2-(dimethoxyphosphoryl)acetate수율 46.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A stirred solution of methyl amino(dimethoxyphosphoryl)acetate (6 g) in dichloromethane (50 mL) is treated with benzoyl chloride (5 g) and the mixture allowed to stand at room temperature for 4 hours. The reaction mixture is washed twice with saturated aqueous sodium bicarbonate solution (75 mL), brine (50 mL), dried over magnesium sulphate and evaporated. The residual pale yellow oil is dissolved in ether (5 mL) and pentane added to give methyl benzoylamino(dimethoxyphosphoryl)acetate (4.25 g) as a white solid.

후처리

  1. washThe reaction mixture is washed twice with saturated aqueous sodium bicarbonate solution (75 mL), brine (50 mL)
  2. dry with materialdried over magnesium sulphate
  3. customevaporated
  4. dissolutionThe residual pale yellow oil is dissolved in ether (5 mL)
  5. additionpentane added

출처 및 근거

ORD 기록
ord-e1b3835f14a0462eb43341f7587aa39d
출처 데이터셋
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06211234B1

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