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7-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-one → 7-fluoro-3,4-dihydro-2H-1,4-benzoxazine

HRID 901831
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HRID 901831 반응식
O=[C:2]1[CH2:7][O:6][C:5]2[CH:8]=[C:9]([F:12])[CH:10]=[CH:11][C:4]=2[NH:3]1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[F:12][C:9]1[CH:10]=[CH:11][C:4]2[NH:3][CH2:2][CH2:7][O:6][C:5]=2[CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 137312957-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-oneHCID 21226445Aluminium lithium hydride

생성물 1

HCID 144229537-fluoro-3,4-dihydro-2H-1,4-benzoxazine수율 65%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

3-Oxo-7-fluoro-3,4-dihydro-2H-benzo[b][1,4]oxazine (2.2 g, 1 eq, 13.1 mmol) obtained in step (ii) in dry THF (10 ml) was added drop wise to a refluxing THF (60 ml) containing LAH (1.5 g, 3 eq, 39.5 mmol). It was further refluxed for 3 h and quenched with ethyl acetate. To this water (1.5 ml), 15% sodium hydroxide (1.5 ml) and water (4.5 ml) were added sequentially. Once Al(OH)3.H2O precipitated out, it was filtered though celite. The filtrate was condensed on rotavapour and chromatographed (ethyl acetate and hexane) to yield 7-fluoro-3,4-dihydro-2H-benzo[b][1,4]oxazine (1.3 g, yield 65%) as yellow oil.

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후처리

  1. temperatureIt was further refluxed for 3 h
  2. customquenched with ethyl acetate
  3. additionTo this water (1.5 ml), 15% sodium hydroxide (1.5 ml) and water (4.5 ml) were added sequentially
  4. customOnce Al(OH)3.H2O precipitated out
  5. filtrationit was filtered though celite
  6. customcondensed on rotavapour
  7. customchromatographed (ethyl acetate and hexane)

출처 및 근거

ORD 기록
ord-f7458281483443b192f3d1980b42c05e
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07365064B2

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