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Ammonia tetrahydrofuran → 3-Cyclopropyl-4-fluorobenzamide

HRID 1808214
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HRID 1808214 반응식
[CH:1]1([C:4]2[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=2[F:13])[C:7](O)=[O:8])[CH2:3][CH2:2]1.[NH3:14].C1COCC1>C1COCC1>[CH:1]1([C:4]2[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=2[F:13])[C:7]([NH2:14])=[O:8])[CH2:3][CH2:2]1
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참가 물질

4

반응물 2

HCID 21982362Ammonia tetrahydrofuranHCID 401517963-Cyclopropyl-4-fluorobenzoic acid

생성물 1

HCID 401517983-Cyclopropyl-4-fluorobenzamide수율 89.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of compound 3-cyclopropyl-4-fluoro-benzoic acid (Preparation 56, 74 g, 0.41 mol, 1 eq) in THF (800 mL) was added N,N′-carbonyldiimidazole (88 g, 0.53 mol, 1.29 eq) at room temperature. The suspension was stirred at room temperature for 3 h, and turned into a brown solution. Ammonia/THF (1 L) was added to the mixture and the resulting mixture was stirred at room temperature overnight. THF was removed in vacuum and the residue was taken up with water (300 mL). The mixture was filtrated and the solid was washed with water (100 mL) and ether (200 mL). The solid was dissolved in DCM (500 mL), dried over sodium sulfate and concentrated in vacuum to title compound as a white solid (66 g, 0.368 mol, 89.7%).

후처리

  1. stirringthe resulting mixture was stirred at room temperature overnight
  2. customTHF was removed in vacuum
  3. filtrationThe mixture was filtrated
  4. washthe solid was washed with water (100 mL) and ether (200 mL)
  5. dissolutionThe solid was dissolved in DCM (500 mL)
  6. dry with materialdried over sodium sulfate

출처 및 근거

ORD 기록
ord-88e189ef37b54406a178115db6d3ef78
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08357711B2

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