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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
ノート
印刷プレビュー

反応式

HRID 901831 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

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.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  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)

出典と根拠

ORDレコード
ord-f7458281483443b192f3d1980b42c05e
出典データセット
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07365064B2

反応ノート

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