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Tetrahydrofuran → 3-Cyclopropyl-4-fluorobenzoic acid

HRID 1808213
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HRID 1808213 반응식
[F:1][C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8]CC)=[O:7])=[CH:4][C:3]=1[CH:13]=[CH2:14].O.[OH-].[Li+].[CH2:18]1COCC1>O>[CH:13]1([C:3]2[CH:4]=[C:5]([CH:11]=[CH:12][C:2]=2[F:1])[C:6]([OH:8])=[O:7])[CH2:14][CH2:18]1
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참가 물질

5

반응물 3

HCID 8028TetrahydrofuranHCID 168937Lithium hydroxide, monohydrateHCID 46941363Ethyl 4-fluoro-3-vinylbenzoate

생성물 1

HCID 401517963-Cyclopropyl-4-fluorobenzoic acid수율 81%

시약·촉매·용매 1

HCID 962Water용매

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온도
40 °C

실험 절차

To a solution of compound 3 ethyl 4-fluoro-3-vinylbenzoate (Preparation 54, 87 g, 0.42 mol, 1 eq) in THF (470 mL) and water (400 mL) was added lithium hydroxide monohydrate (35.1 g, 0.84 mol, 2.0 eq). The resulting mixture was stirred at 40° C. overnight. THF was removed in vacuum, then 6N hydrogen chloride solution was added dropwise until pH=2. The mixture was extracted with ethyl acetate (3×600 mL). The organic phase was dried over sodium sulfate and concentrated in vacuo to give title compound as a white solid (60.8 g, 0.34 mol, 81%).

후처리

  1. customTHF was removed in vacuum
  2. addition6N hydrogen chloride solution was added dropwise until pH=2
  3. extractionThe mixture was extracted with ethyl acetate (3×600 mL)
  4. dry with materialThe organic phase was dried over sodium sulfate
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-0a93e51849324a25b296aedcb8cd70b7
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08357711B2

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