Methyl 2,4-dinitro-5-fluorophenoxyacetate → 7-Fluoro-6-amino-2H-1,4-benzoxazin-3(4H)-one

HRID 2255179ノート

反応式

HRID 2255179 の反応式
[N+:1]([C:4]1[CH:15]=[C:14]([N+:16]([O-])=O)[C:13]([F:19])=[CH:12][C:5]=1[O:6][CH2:7][C:8](OC)=[O:9])([O-])=O>C(O)(=O)C.CCOC(C)=O.[Fe]>[NH2:16][C:14]1[C:13]([F:19])=[CH:12][C:5]2[O:6][CH2:7][C:8](=[O:9])[NH:1][C:4]=2[CH:15]=1

参加物

5

反応物 1

HCID 14423669Methyl 2,4-dinitro-5-fluorophenoxyacetate

生成物 1

HCID 103133897-Fluoro-6-amino-2H-1,4-benzoxazin-3(4H)-one収率 60%

試薬・触媒・溶媒 3

HCID 23925Iron触媒HCID 176Acetic Acid溶媒2 回HCID 8857Ethyl Acetate溶媒

実験手順

To a suspension of 12.2 g (0.22 mol) of iron powder in 100 ml of 5% aqueous acetic acid was added dropwise a solution of 10.0 g (36.5 mmol) of methyl 2,4-dinitro-5-fluorophenoxyacetate in 100 ml of EtOAc and 100 ml of glacial acetic acid. The reaction mixture was stirred at room temperature for 18 hours. The iron was removed by suction filtration through a small pad of Celite® and the filter pad was rinsed with 50 ml of EtOAc. The filtrate was transferred to a separatory funnel and the phases were separated. The aqueous layer was extracted with EtOAc (3×50 ml) and the combined organic phases were washed with sodium bicarbonate (2×50 ml), dried over Na2SO4 and filtered. The solvent was removed from the filtrate in vacuo to yield 3.9 g (60% yield) of 6-amino-7-fluoro-2H-1,4-benzoxazin-3(4H)-one as a brown solid.

後処理

  1. customThe iron was removed by suction filtration through a small pad of Celite®
  2. washthe filter pad was rinsed with 50 ml of EtOAc
  3. customThe filtrate was transferred to a separatory funnel
  4. customthe phases were separated
  5. extractionThe aqueous layer was extracted with EtOAc (3×50 ml)
  6. washthe combined organic phases were washed with sodium bicarbonate (2×50 ml)
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. customThe solvent was removed from the filtrate in vacuo

出典と根拠

ORDレコード
ord-581ebe0867804e2d9a5610259bf7c871
出典データセット
uspto-grants-1993_08
特許番号
US05238908

反応ノート

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