Ethanol → Ethyl 3-[(2,6-dinitrophenyl)amino]-2,2-difluoropropanoate

HRID 1628518ノート

反応式

HRID 1628518 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([N+:10]([O-:12])=[O:11])[C:5]=1[NH:13][CH2:14][C:15]([F:20])([F:19])[C:16]([OH:18])=[O:17])([O-:3])=[O:2].S(=O)(=O)(O)O.C(=O)([O-])O.[Na+].[CH2:31](O)[CH3:32]>>[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([N+:10]([O-:12])=[O:11])[C:5]=1[NH:13][CH2:14][C:15]([F:19])([F:20])[C:16]([O:18][CH2:31][CH3:32])=[O:17])([O-:3])=[O:2]

参加物

5

反応物 4

HCID 702EthanolHCID 1118Sulfuric AcidHCID 516892Sodium BicarbonateHCID 86632897HCID 86632897、化合物

生成物 1

HCID 86632898Ethyl 3-[(2,6-dinitrophenyl)amino]-2,2-difluoropropanoate収率 76%

反応条件

温度
100 °C

実験手順

To a solution of 3-[(2,6-dinitrophenyl)amino]-2,2-difluoropropanoic acid (3.52 g, 12.09 mmol) in ethanol (30.0 mL) was added sulfuric acid (4 mL) at 0° C. The reaction mixture was stirred at 100° C. for 1 hr. After cooling, the reaction mixture was neutralized with aqueous saturated sodium hydrogen carbonate and the solvent was removed. The residue was extracted with ethyl acetate (×3) The combined organic layer was washed with brine (×1), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with a 0-20% ethyl acetate/n-hexane gradient mixture to give the title compound as a yellow oil (2.94 g, 9.210 mmol, 76%).

後処理

  1. temperatureAfter cooling
  2. customthe solvent was removed
  3. extractionThe residue was extracted with ethyl acetate (×3) The combined organic layer
  4. washwas washed with brine (×1)
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by silica gel column chromatography
  9. washeluting with a 0-20% ethyl acetate/n-hexane gradient mixture

出典と根拠

ORDレコード
ord-f693c806475d4f8b8daac606d68b3262
出典データセット
uspto-grants-2014_07
特許番号
US08785460B2

反応ノート

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