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Methane → Ethyl-2-(2-ethoxytetrahydrofuran-3-yl)-2-oxoacetate

HRID 78750
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인쇄 미리보기

반응식

HRID 78750 반응식
[CH2:1]([O:3][C:4](=[O:12])[C:5]([C:7]1[CH2:11][CH2:10][O:9][CH:8]=1)=[O:6])[CH3:2].C.[CH2:14]([OH:16])[CH3:15]>>[CH2:1]([O:3][C:4](=[O:12])[C:5]([CH:7]1[CH2:11][CH2:10][O:9][CH:8]1[O:16][CH2:14][CH3:15])=[O:6])[CH3:2]
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참가 물질

4

반응물 3

HCID 297MethaneHCID 702EthanolHCID 11571862HCID 11571862, 화합물

생성물 1

HCID 67607633Ethyl-2-(2-ethoxytetrahydrofuran-3-yl)-2-oxoacetate

반응 조건

온도
45 °C

실험 절차

Ethyl-2-(4,5-dihydrofuran-3-yl)-2-oxoacetate (10 g) was dissolved in Ethanol (50 ml) and Methane sulphoic acid (0.1 ml) was added to it. The reaction mass was stirred at 40-50° C. for 12 hrs. Reaction mass was concentrated to residue under vacuum. Residue was dissolved in dichloromethane (50 ml) and washed with water (50 ml). Reaction mass was concentrated to residue to get ethyl-2-(2-ethoxytetrahydrofuran-3-yl)-2-oxoacetate (Yield 9.2 g).

후처리

  1. customReaction mass
  2. concentrationwas concentrated to residue under vacuum
  3. dissolutionResidue was dissolved in dichloromethane (50 ml)
  4. washwashed with water (50 ml)
  5. customReaction mass
  6. concentrationwas concentrated to residue

출처 및 근거

ORD 기록
ord-62a1df65a239421ea94cf65b148ce0c3
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08841467B2

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