참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Hydrazinium chloride | HCID 115031 | — |
| 반응물 | Ethyl ethoxymethylene-3-oxo-4,4,4-trifluorobutyrate | HCID 6185754 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | Ethyl 3-(Trifluoromethyl)pyrazole-4-carboxylate | HCID 596095 | — |
반응 단계
To a suspension of hydrazine hydrochloride (10 g, 147 mmol) in EtOH (500 mL), DIPEA (45.3 mL, 267 mmol) was added slowly at −20° C. and stirred for 10 minutes. Then 2-[1-ethoxy-meth-(E)-ylidene]-4,4,4-trifluoro-3-oxo-butyric acid ethyl ester (Preparation 96 Step 1, 32 g, 133.33 mmol) was added to above solution and the resulting mixture was stirred at room temperature for 16 hours. The reaction mixture was concentrated under reduced pressure and residue was partitioned between EtOAc (200 mL) and water (50 mL). The organic layer was washed with water (25 mL), dried (Na2SO4) and evaporated in vacuo. The crude material was purified by silica gel column chromatography eluting with Hexane:EtOAc 90:10 to afford the title compound as off white solid (43%, 13 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09163021B2 |
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| 출처 데이터셋 | uspto-grants-2015_10 |
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| ORD ID | ord-18b821e71bac48ef9446089e8e737330 |
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| 출처 메모 | uspto-grants-2015_10 |
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