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Ethanol → HCID 67609650, 화합물

HRID 78746
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HRID 78746 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].[CH2:13]([OH:15])[CH3:14].[Br:16]N1C(=O)CCC1=O>ClCCl>[CH2:1]([O:3][C:4](=[O:12])[C:5]([C:7]1([Br:16])[CH2:11][CH2:10][O:9][CH:8]1[O:15][CH2:13][CH3:14])=[O:6])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 67184N-bromobutanimideHCID 11571862HCID 11571862, 화합물

생성물 1

HCID 67609650HCID 67609650, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
7.5 °C

실험 절차

Ethyl-2-(4,5-dihydrofuran-3-yl)-2-oxoacetate (100 g) was dissolved in dichloromethane (500 ml) and Ethanol (150 ml) was added to reaction mass and then reaction mass was cooled to 5 to 10° C. N-bromosuccinimide (115 g) was added lot wise by maintaining temp below 10° C. Reaction mass was then stirred at 20-30° C. till completion of reaction. Reaction mass was washed with sodium bicarbonate solution (8%, 3×400 ml). Reaction mass was then concentrated to residue to get Ethyl-2-(3-bromo-2-ethoxytetrahydrofuran-3-yl)-2-oxoacetate (Yield 170 g).

후처리

  1. customreaction mass
  2. temperatureby maintaining temp below 10° C
  3. customReaction mass
  4. customReaction mass
  5. washwas washed with sodium bicarbonate solution (8%, 3×400 ml)
  6. customReaction mass
  7. concentrationwas then concentrated to residue

출처 및 근거

ORD 기록
ord-cef9affb204c4359a1873eeea5425a27
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08841467B2

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