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Trimethyl Phosphate → Ethyl 3-difluoromethyl-1-methyl-4-pyrazole carboxylate

HRID 2244774
ノート
印刷プレビュー

反応式

HRID 2244774 の反応式
[CH2:1]([O:3][C:4]([C:6]1[C:7]([CH:11]([F:13])[F:12])=[N:8][NH:9][CH:10]=1)=[O:5])[CH3:2].P(OC)(OC)(O[CH3:17])=O>>[CH2:1]([O:3][C:4]([C:6]1[C:7]([CH:11]([F:12])[F:13])=[N:8][N:9]([CH3:17])[CH:10]=1)=[O:5])[CH3:2]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 10541Trimethyl PhosphateHCID 178469922HCID 178469922、化合物

生成物 1

HCID 11644126Ethyl 3-difluoromethyl-1-methyl-4-pyrazole carboxylate収率 64%

反応条件

温度
180 °C

実験手順

A mixture of 5.7 g of 3-difluoromethyl-1H-pyrazole-4-carboxylic acid ethyl ester (30 mmol) and 25 ml of trimethyl phosphate (214 mmol) is stirred at a temperature of 180° C. for 18 hours. 250 ml of an ice-water mixture are then added. The resulting reaction product is filtered, washed with water and dissolved in 50 ml of ethyl acetate. The organic phase is washed with 50 ml of saturated sodium chloride solution and dried over sodium sulfate and concentrated by evaporation. 3.9 g (64% of theory) of 3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid ethyl ester are obtained in the form of crystals (m.p. 59-60° C.).

後処理

  1. customThe resulting reaction product
  2. filtrationis filtered
  3. washwashed with water
  4. dissolutiondissolved in 50 ml of ethyl acetate
  5. washThe organic phase is washed with 50 ml of saturated sodium chloride solution
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated by evaporation

出典と根拠

ORDレコード
ord-459e59df174945eb9b61201539530d07
出典データセット
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07678924B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート