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Methylhydrazine → ethyl 2-(1,3,5-trimethyl-1H-pyrazol-4-yl)acetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methylhydrazine | HCID 6061 | — |
| 反応物 | Ethyl 3-acetyl-4-oxopentanoate | HCID 87820 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | ethyl 2-(1,3,5-trimethyl-1H-pyrazol-4-yl)acetate | HCID 16394807 | 73.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08202873B2 |
| 出典データセット | uspto-grants-2012_06 |
| ORD ID | ord-2d95a319eeab4885851635057c0e2465 |
| 出典メモ | uspto-grants-2012_06 |