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Ethanol → HCID 10926216, 화합물

HRID 975486
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HRID 975486 반응식
ClC(O[CH2:5][CH:6](C)C)=O.[C:9]([O:13][C:14]([NH:16][CH2:17][P:18]([CH2:21][NH:22][C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])(=[O:20])[OH:19])=[O:15])([CH3:12])([CH3:11])[CH3:10].C(O)C.C(N(CC)CC)C>C(Cl)Cl>[C:9]([O:13][C:14]([NH:16][CH2:17][P:18]([CH2:21][NH:22][C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])(=[O:19])[O:20][CH2:5][CH3:6])=[O:15])([CH3:12])([CH3:11])[CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 702EthanolHCID 8471TriethylamineHCID 62365Isobutyl chloroformateHCID 11120883HCID 11120883, 화합물

생성물 1

HCID 10926216HCID 10926216, 화합물수율 53%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Isobutyl chloroformate (1.50 ml, 11.48 mmol) is added dropwise with stirring at 0° C. to a solution of the phosphinic acid 1 (3.200 g, 9.88 mmol) in a mixture of methylene chloride (50 ml), ethanol (3.00 ml, 51.59 mmol), triethylamine (1.40 ml, 10.06 mmol) and N,N-dimethylpyridine (10 mg). After 90 minutes, the reaction solution is extracted with saturated aqueous ammonium chloride solution (30 ml) and saturated aqueous KHCO3 solution (30 ml). The organic phase is dried over Na2SO4 and concentrated under reduced pressure. After purification by column chromatography on silica gel (ethyl acetate/heptane=3:2), the phosphinic acid ester 3 (1.840 g, 53% of theory) is obtained. See above spectroscopic data.

후처리

  1. extractionthe reaction solution is extracted with saturated aqueous ammonium chloride solution (30 ml) and saturated aqueous KHCO3 solution (30 ml)
  2. dry with materialThe organic phase is dried over Na2SO4
  3. concentrationconcentrated under reduced pressure
  4. customAfter purification by column chromatography on silica gel (ethyl acetate/heptane=3:2)

출처 및 근거

ORD 기록
ord-6a0af0fb985c4d0386328b373eb6fb1a
출처 데이터셋
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05608098

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