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HCID 86756551, 화합물 → HCID 22011772, 화합물

HRID 1532951
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HRID 1532951 반응식
C[O:2][C:3](=[O:27])/[C:4](/[CH:10]([P:19]([O:24][CH2:25][CH3:26])([O:21][CH2:22][CH3:23])=[O:20])[P:11]([O:16][CH2:17][CH3:18])([O:13][CH2:14][CH3:15])=[O:12])=[CH:5]\[C:6]([O:8]C)=[O:7]>[OH-].[Na+]>[CH2:22]([O:21][P:19]([CH:10]([P:11]([O:16][CH2:17][CH3:18])([O:13][CH2:14][CH3:15])=[O:12])/[C:4](=[CH:5]/[C:6]([OH:8])=[O:7])/[C:3]([OH:27])=[O:2])([O:24][CH2:25][CH3:26])=[O:20])[CH3:23]
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참가 물질

3

반응물 1

HCID 86756551HCID 86756551, 화합물

생성물 1

HCID 22011772HCID 22011772, 화합물

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

A solution of 12.7 g of 2-[bis(diethoxyphosphoryl)methyl]maleic acid dimethyl ester in 76.8 ml of 1 N sodium hydroxide is kept under stirring for 96 hours, then the reaction mixture is washed twice with ethyl ether and is brought to pH 8.5 with 37% hydrochloric acid. The mixture is then concentrated to dryness and redissolved in 50 ml of methanol. After filtration of the formed sodium chloride, the solvent is evaporated under reduced pressure. The residue is treated with 125 ml of acetone, to give, after filtration, 11.5 g of the product as disodium salt.

후처리

  1. washthe reaction mixture is washed twice with ethyl ether
  2. concentrationThe mixture is then concentrated to dryness
  • dissolutionredissolved in 50 ml of methanol
  • filtrationAfter filtration of the formed sodium chloride
  • customthe solvent is evaporated under reduced pressure
  • additionThe residue is treated with 125 ml of acetone
  • customto give
  • filtrationafter filtration, 11.5 g of the product as disodium salt
  • 출처 및 근거

    ORD 기록
    ord-58ab8f8022b14eeb951fc99c8da67f18
    출처 데이터셋
    uspto-grants-2001_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06207655B1

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