Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432115생성일: 2026년 10월 26일
Diethyl methylmalonate → 1-(3-bromophenyl)-5-hydroxy-4-methyl-1,2-dihydro-3H-pyrazol-3-one
https://huagongshe.com/reaction/432115
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Diethyl methylmalonate | HCID 11857 | — |
| 반응물 | 3-Bromophenylhydrazine hydrochloride | HCID 33757 | — |
| 반응물 | Sodium ethoxide | HCID 2723922 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 1-(3-bromophenyl)-5-hydroxy-4-methyl-1,2-dihydro-3H-pyrazol-3-one | HCID 22351447 | 10.4% |
반응 단계
To a suspension of 1-(3-bromophenyl)hydrazine hydrochloride (1.0 g, 4.47 mmol) in ethanol (8.9 mL) was added dropwise 2.0 M sodium ethoxide in ethanol (0.77 mL, 9.84 mmol, 2.2 eq.). Diethyl 2-methylmalonate (0.85 mL, 4.92 mmol, 1.1 eq.) was then added. The reaction mixture was stirred at 90° C. for 16 hours and then quenched with 2 N aqueous hydrochloric acid (50 mL). The reaction was extracted with ethyl acetate (3×50 mL), and the combined organic layers were dried (MgSO4), filtered, and evaporated under reduced pressure. Purification using MPLC (Biotage) eluted with 3:1 v/v ethyl acetate-hexane gave the desired product as a white solid (125 mg, 0.46 mmol, 10.4% yield). MS LC-MS (ES MH+=269/271); TLC (Rf=0.10, 50% ethyl acetate-hexane).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06660752B2 |
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| 출처 데이터셋 | uspto-grants-2003_12 |
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| ORD ID | ord-c0a2637b7cfc4f828ad4965f769c119f |
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| 출처 메모 | uspto-grants-2003_12 |
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