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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → Ethyl 2-pyridin-3-ylpropanoate

HRID 1600840
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HRID 1600840 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH:2]=1.[Li+].[CH3:14]C([N-]C(C)C)C.O.CCOCC>C1COCC1>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH:7]([CH3:14])[C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 3283Diethyl EtherHCID 96490Ethyl 3-pyridylacetateHCID 2724682Lithium diisopropylamide

생성물 1

HCID 10726035Ethyl 2-pyridin-3-ylpropanoate수율 62.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

Ethyl 3-pyridylacetate (12.2 g, 73.9 mmol) in THF (30 ml) was added to LDA (81 mmol) in THF (150 ml) over 10 min at -78° C. After 1 h Mel (5.1 ml, 81 mmol) was added to the yellow suspension and the mixture brought to room temperature. H2O (300 ml) and ether (300 ml) was added, the mixture separated, and the organic layer washed with H2O and brine, dried and evaporated to give ethyl 2-(3-pyridyl)propanoate (8.3 g) as a yellow oil.

후처리

  1. additionAfter 1 h Mel (5.1 ml, 81 mmol) was added to the yellow suspension
  2. custombrought to room temperature
  3. customthe mixture separated
  4. washthe organic layer washed with H2O and brine
  5. customdried
  6. customevaporated

출처 및 근거

ORD 기록
ord-e1e67158406e495f8ce377dc45162e4c
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05977116

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