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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220457생성일: 2026년 10월 26일

Methylhydrazine → ethyl 2-(1,3,5-trimethyl-1H-pyrazol-4-yl)acetate

https://huagongshe.com/reaction/220457

반응식

참여 물질

역할이름HCID투입량
반응물MethylhydrazineHCID 6061—
반응물Ethyl 3-acetyl-4-oxopentanoateHCID 87820—
용매Acetic AcidHCID 176—
생성물ethyl 2-(1,3,5-trimethyl-1H-pyrazol-4-yl)acetateHCID 1639480773.2%

반응 단계

Dissolve 3-acetyl-4-oxopentanoic acid ethyl ester (3.35 g, 19.5 mmol) in glacial acetic acid (20 mL) and add methylhydrazine (1.13 mL, 21.4 mmol) dropwise. Stir the resulting mixture at room temperature for 16 hr. Concentrate and partition the residue between ethyl acetate (100 mL) and saturated aqueous sodium bicarbonate solution (50 mL). Separate organic layer, dry (sodium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 7:3 hexanes:ethyl acetate) to give (1,3,5-trimethyl-1H-pyrazol-4-yl)-acetic acid ethyl ester (2.8 g, 73%) as an oil. 1H NMR (CDCl3) δ 4.08 (q, 2H), 3.67 (s, 3H), 3.29 (s, 2H), 2.18 (s, 6H), 1.21 (t, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202873B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-2d95a319eeab4885851635057c0e2465
출처 메모uspto-grants-2012_06