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HRID 220457作成日:2026年10月26日

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

https://huagongshe.com/reaction/220457

反応式

関与物質

役割名称HCID仕込み量
反応物MethylhydrazineHCID 6061—
反応物Ethyl 3-acetyl-4-oxopentanoateHCID 87820—
溶媒Acetic AcidHCID 176—
生成物ethyl 2-(1,3,5-trimethyl-1H-pyrazol-4-yl)acetateHCID 1639480773.2%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202873B2
出典データセットuspto-grants-2012_06
ORD IDord-2d95a319eeab4885851635057c0e2465
出典メモuspto-grants-2012_06