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Ethyl trifluoroacetate → 5,5-Diethoxy-1,1,1-trifluoro-pent-3-yn-2-one

HRID 1952573
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HRID 1952573 반응식
[CH2:1]([O:3][CH:4]([O:7][CH2:8][CH3:9])[C:5]#[CH:6])[CH3:2].[Li]CCCC.C([O:17][C:18](=O)[C:19]([F:22])([F:21])[F:20])C>C1COCC1>[CH2:1]([O:3][CH:4]([O:7][CH2:8][CH3:9])[C:5]#[C:6][C:18](=[O:17])[C:19]([F:22])([F:21])[F:20])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 9794Ethyl trifluoroacetateHCID 662853,3-DiethoxypropyneHCID 178418339Butyllithium

생성물 1

HCID 109770935,5-Diethoxy-1,1,1-trifluoro-pent-3-yn-2-one

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of 3,3-Diethoxy-propyne (0.98 g, 7.64 mmol) in THF (20 ml) was cooled to −78 C under Ar. A solution of n-BuLi (2.0M in cyclohexane, 4.2 ml, 8.40 mmol) was added. After 30 min., Trifluoroacetic acid ethyl ester (1.19 g, 8.40 mmol) was added. After 1 h, the reaction was quenched by dilution with 1N HCl, warmed to room temperature and extracted into EtOAc. The organic layer was washed with brine, dried over sodium sulfate, filtered and evaporated. The residue was purified by flash chromatography (0-40% EtOAc in Hexanes) to give product, 0.51 g (30%).

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후처리

  1. temperaturewas cooled to −78 C under Ar
  2. waitAfter 1 h
  3. customthe reaction was quenched by dilution with 1N HCl
  4. extractionextracted into EtOAc
  5. washThe organic layer was washed with brine
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. customevaporated
  9. customThe residue was purified by flash chromatography (0-40% EtOAc in Hexanes)
  10. customto give product, 0.51 g (30%)

출처 및 근거

ORD 기록
ord-f8e6773304a54db194ed875d379c60cd
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08404859B2

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