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Tetrabutylammonium Fluoride → (E)-methyl 4-(3,3,3-trifluoroprop-1-enyl)-2-methoxybenzoate

HRID 2102911
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HRID 2102911 반응식
CCCC[N+](CCCC)(CCCC)CCCC.[F-].[CH:19]([C:21]1[CH:30]=[CH:29][C:24]([C:25]([O:27][CH3:28])=[O:26])=[C:23]([O:31][CH3:32])[CH:22]=1)=O.[F:33][C:34]([F:51])([F:50])[CH2:35]P(=O)(C1C=CC=CC=1)C1C=CC=CC=1>C1COCC1>[F:33][C:34]([F:51])([F:50])/[CH:35]=[CH:19]/[C:21]1[CH:30]=[CH:29][C:24]([C:25]([O:27][CH3:28])=[O:26])=[C:23]([O:31][CH3:32])[CH:22]=1
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참가 물질

5

반응물 3

HCID 2724141Tetrabutylammonium FluorideHCID 11323568Diphenyl(2,2,2-trifluoroethyl)phosphine oxideHCID 18510332Methyl 4-formyl-2-methoxybenzoate

생성물 1

HCID 68702754(E)-methyl 4-(3,3,3-trifluoroprop-1-enyl)-2-methoxybenzoate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

MS 4 Å (powder, 16 g) was added to a 1 M solution of TBAF in THF (20 mL, 20 mmol), and the mixture was stirred at room-temperature overnight under an argon atmosphere. To the mixture were added a solution of methyl 4-formyl-2-methoxybenzoate (420 mg, 0.0022 mol) and 2,2,2-trifluoroethyldiphenylphosphine oxide (1.23 g, 0.00432 mol) in THF (20 mL). After the mixture was stirred for 2 h, MS 4 Å was removed by filtration. The filtrate was concentrated and water (120 mL) was added. The mixture was extracted with AcOEt. The extract was washed with brine, dried (Na2SO4), and concentrated. The residue was purified by column chromatography on silica gel using AcOEt-hexane (0-15%) as eluent to give (E)-methyl 4-(3,3,3-trifluoroprop-1-enyl)-2-methoxybenzoate as a white solid, followed by (Z)-methyl 4-(3,3,3-trifluoroprop-1-enyl)-2-methoxybenzoate as a colorless oil.

후처리

  1. stirringAfter the mixture was stirred for 2 h
  2. customMS 4 Å was removed by filtration
  3. concentrationThe filtrate was concentrated
  4. additionwater (120 mL) was added
  5. extractionThe mixture was extracted with AcOEt
  6. washThe extract was washed with brine
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated
  9. customThe residue was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-fcddb2ce6a4846f08d649ce672a01d31
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07576099B2

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