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Water → 4-benzyl-8,9-difluoro-3,4-dihydro-1,4-benzoxazepin-5(2H)-one

HRID 548668
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HRID 548668 반응식
[H-].[Na+].[CH2:3]([N:10]([CH2:22][CH2:23][OH:24])[C:11](=[O:21])[C:12]1[CH:17]=[CH:16][C:15]([F:18])=[C:14]([F:19])[C:13]=1F)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.O>CN(C=O)C>[CH2:3]([N:10]1[C:11](=[O:21])[C:12]2[CH:17]=[CH:16][C:15]([F:18])=[C:14]([F:19])[C:13]=2[O:24][CH2:23][CH2:22]1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 24758Sodium hydrideHCID 57663176N-benzyl-2,3,4-trifluoro-N-(2-hydroxyethyl)benzamide

생성물 1

HCID 576631824-benzyl-8,9-difluoro-3,4-dihydro-1,4-benzoxazepin-5(2H)-one수율 73.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Sodium hydride (25 mg, 0.615 mmol, 60% dispersion in mineral oil) was added slowly to a solution of N-benzyl-2,3,4-trifluoro-N-(2-hydroxyethyl)benzamide (190 mg, 0.615 mmol) in DMF (3 mL) and the pale yellow solution was stirred at RT for 16 hours. Water was added to the reaction and the mixture was subsequently extracted with DCM (4×30 mL). The combined organic phases were washed with water (3×20 mL) and saturated brine solution then dried (MgSO4), filtered and evaporated to give the desired product as a colourless oil (130 mg). 1H NMR δ (CDCl3): 3.5 (t, 2H), 4.3 (t, 2H), 4.8 (s, 2H), 6.92 (dd, 1H), 7.3-7.4 (m, 5H), 7.7 (m, 1H)

후처리

  1. extractionthe mixture was subsequently extracted with DCM (4×30 mL)
  2. washThe combined organic phases were washed with water (3×20 mL) and saturated brine solution
  3. dry with materialthen dried (MgSO4)
  4. filtrationfiltered
  5. customevaporated

출처 및 근거

ORD 기록
ord-d5b39d49d35141ab89520e1c63a52848
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07943607B2

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