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

HRID 2244774
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인쇄 미리보기

반응식

HRID 2244774 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 10541Trimethyl PhosphateHCID 178469922HCID 178469922, 화합물

생성물 1

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

반응 조건

온도
180 °C

실험 절차

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.).

후처리

  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

출처 및 근거

ORD 기록
ord-459e59df174945eb9b61201539530d07
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07678924B2

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