Ethyl bromopyruvate → Ethyl 2-(trifluoromethyl)-1,3-thiazole-4-carboxylate

HRID 1654207

反応式

HRID 1654207 の反応式
Br[CH2:2][C:3](=O)[C:4]([O:6][CH2:7][CH3:8])=[O:5].[F:10][C:11]([F:16])([F:15])[C:12]([NH2:14])=[S:13]>C(O)C>[F:10][C:11]([F:16])([F:15])[C:12]1[S:13][CH:2]=[C:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])[N:14]=1

参加物

4

実験手順

A mixture of ethyl bromopyruvate (6.82 g), 2,2,2-trifluorothioacetamide (4.52 g) and ethanol (30 ml) was refluxed for 3 hours. The reaction mixture was cooled, then ethanol was distilled off under reduced pressure. To the residue was added water (40 ml), which was subjected to extraction with ethyl acetate (60 ml×2). The extract solution was washed with water (40 ml) and dried over magnesium sulfate, then the solvent was distilled off under reduced pressure. The residue was subjected to a silica gel chromatography (2.5×45 cm), eluting with ethyl acetate-hexane (1:5). The desired fraction was concentrated to give ethyl 2-trifluoromethyl-4-thiazolecarboxylate (2.2 g) as pale yellow needles.

後処理

  1. temperaturewas refluxed for 3 hours
  2. temperatureThe reaction mixture was cooled
  3. distillationethanol was distilled off under reduced pressure
  4. additionTo the residue was added water (40 ml), which
  5. extractionwas subjected to extraction with ethyl acetate (60 ml×2)
  6. washThe extract solution was washed with water (40 ml)
  7. dry with materialdried over magnesium sulfate
  8. distillationthe solvent was distilled off under reduced pressure
  9. washeluting with ethyl acetate-hexane (1:5)
  10. concentrationThe desired fraction was concentrated

出典と根拠

ORDレコード
ord-4fe85517102648258dce034629f944e0
出典データセット
uspto-grants-1995_04
特許番号
US05405861

関連ノート

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