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Ethanol → Ethyl 3-(difluoromethyl)-1-(2-propenyl)-1H-pyrazole-4-carboxylate

HRID 1588780
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반응식

HRID 1588780 반응식
[OH-].[K+].[F:3][CH:4]([F:13])[C:5]1[C:9]([C:10]([OH:12])=[O:11])=[CH:8][NH:7][N:6]=1.[CH2:14](Br)[CH:15]=[CH2:16].[CH2:18](O)[CH3:19]>>[F:13][CH:4]([F:3])[C:5]1[C:9]([C:10]([O:12][CH2:18][CH3:19])=[O:11])=[CH:8][N:7]([CH2:14][CH:15]=[CH2:16])[N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 702Ethanol2회HCID 7841Allyl bromideHCID 14797Potassium HydroxideHCID 178524804HCID 178524804, 화합물

생성물 1

HCID 19754742Ethyl 3-(difluoromethyl)-1-(2-propenyl)-1H-pyrazole-4-carboxylate

실험 절차

To a solution of potassium hydroxide (3.5 g) in ethanol (50 mL) at 0° C. was added dropwise the ethyl ester of 3-(difluoromethyl)-1H-pyrazole-4-carboxylic acid (10.1 g) in ethanol (50 mL), followed by dropwise addition of allyl bromide (4.6 mL). The mixture was stirred overnight, partitioned between ether and 2N HCl. The ether layer was dried (MgSO4) and concentrated in vacuo leaving an oil (11.4 g). The oil was distilled (Kugelrohr 80-85 ° C., 0.3 mm) to give the isomer of the desired product as an oil (2.6 g). Distillation was continued (100-105 ° C., 0.3 mm) to give the desired compound as a clear colorless oil (8.0 g).

후처리

  1. custompartitioned between ether and 2N HCl
  2. dry with materialThe ether layer was dried (MgSO4)
  3. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-335b7abd461b46faa4fe4083b475eb95
출처 데이터셋
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05223526

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