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Methyl 2-(5-fluoro-2-nitrophenoxy)acetate → 7-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-one

HRID 1441099
ノート
印刷プレビュー

反応式

HRID 1441099 の反応式
[F:1][C:2]1[CH:3]=[CH:4][C:5]([N+:14]([O-])=O)=[C:6]([CH:13]=1)[O:7][CH2:8][C:9](OC)=[O:10]>[Pd].CCO>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[NH:14][C:9](=[O:10])[CH2:8][O:7][C:6]=2[CH:13]=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 1

HCID 2779697Methyl 2-(5-fluoro-2-nitrophenoxy)acetate

生成物 1

HCID 137312957-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-one

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

To 500 mg of 5% Pd/C in a Parr bottle was added 100 ml of EtOH followed by 5.0 g (21.8 mmol) of methyl 5-fluoro-2-nitrophenoxyacetate. The flask was placed in a Parr Apparatus, evacuated and then charged with hydrogen. The suspension was then shaken for 2 hours. After evacuating the flask and recharging with nitrogen, the solids were removed by vacuum filtration through Celite®. Since some product does precipitate, the filter cake is repeatedly rinsed with EtOAc (200 ml). The filtrate is refluxed for 4 hours and then evaporated to dryness in vacuo to give the desired material, 7-fluoro-2H-1,4-benzoxazin-3(4H)-one, as a white solid (m.p. 201°-202° C.) in quantitative yield.

後処理

  1. customevacuated
  2. additioncharged with hydrogen
  3. customAfter evacuating the flask
  4. customthe solids were removed by vacuum filtration through Celite®
  5. washthe filter cake is repeatedly rinsed with EtOAc (200 ml)
  6. temperatureThe filtrate is refluxed for 4 hours
  7. customevaporated to dryness in vacuo

出典と根拠

ORDレコード
ord-c44514e13ceb41aa93ca7b71debc5c81
出典データセット
uspto-grants-1996_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05502027

反応ノート

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