Methyl p-toluenesulfonate → 3-Methoxy-4,4,4-trifluoro-2-butenoic acid ethyl ester

HRID 23322

反応式

HRID 23322 の反応式
[C:1](=O)([O-])[O-].[Cs+].[Cs+].[F:7][C:8]([F:18])([F:17])[C:9](=[O:16])[CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12].S(C1C=CC(C)=CC=1)(OC)(=O)=O>CN(C)C=O>[CH3:1][O:16][C:9]([C:8]([F:17])([F:18])[F:7])=[CH:10][C:11]([O:13][CH2:14][CH3:15])=[O:12]

参加物

5

反応条件

温度
20 °C

実験手順

Cesium carbonate (132.8 g) was added to a mixture of ethyl 4,4,4-trifluoroacetoacetate (75.0 g) and dimethylformamide (400 ml). The reaction mixture was heated to 20° C. for 30 minutes. A mixture of methyl tosylate (83.4 g) and dimethylformamide (150 ml) was added to the resulting reaction mixture within 40 minutes. The mixture was heated for 3 hours and cooled to room temperature. Upon dilution with water (800 ml) the reaction mixture was extracted with diethyl ether three times. The combined organic phases were washed with water and dried. The mixture was concentrated and the residue distilled under reduced pressure to yield the product as a clear liquid (48.5 g, 60%) with a boiling point of 62-70° C. at 12 mm.

後処理

  1. additionwas added to the resulting reaction mixture within 40 minutes
  2. temperatureThe mixture was heated for 3 hours
  3. temperaturecooled to room temperature
  4. extractionUpon dilution with water (800 ml) the reaction mixture was extracted with diethyl ether three times
  5. washThe combined organic phases were washed with water
  6. customdried
  7. concentrationThe mixture was concentrated
  8. distillationthe residue distilled under reduced pressure

出典と根拠

ORDレコード
ord-5f3d8a5e0cf347a9a8f5547118f9154a
出典データセット
uspto-grants-2005_02
特許番号
US06852673B2

関連ノート

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