化工社化工社 化学情報印刷レポート · 研究参考用
Sulfuryl chloride → ethyl 3-tert-butyl-4-chloro-1-methyl-1H-pyrazole-5-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sulfuryl chloride | HCID 24648 | — |
| 反応物 | ethyl 3-(tert-butyl)-1-methyl-1H-pyrazole-5-carboxylate | HCID 2799344 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | ethyl 3-tert-butyl-4-chloro-1-methyl-1H-pyrazole-5-carboxylate | HCID 67412028 | — |
反応手順
To a solution of 5-tert-butyl-2-methyl-pyrazole-3-carboxylic acid ethyl ester (2.10 g, 10.0 mmol) in 25 mL of DCM was added sulfuryl chloride (1.05 mL, 13.0 mmol) slowly under Ar. After stirring at room temperature for 3 h under Ar, the resulting mixture was treated with DCM (30 mL), washed with ice H2O, saturated aqueous NaHCO3 and brine, and dried with Na2SO4. Removal of the solvent under reduced pressure yielded the title compound as a white solid. 1H-NMR (400 MHz, CDCl3) δ: 4.40 (q, J=7.2 Hz, 2H), 4.07 (s, 3H), 1.42 (t, J=7.2 Hz, 3H), 1.40 (s, 9H). Mass Spectrum (LCMS, ESI pos.) Calculated For C11H17ClN2O2: 245.1 (M+H), Measured: 245.1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09023846B2 |
| 出典データセット | uspto-grants-2015_05 |
| ORD ID | ord-5f61c25fc0fd4378b046af5a34fad283 |
| 出典メモ | uspto-grants-2015_05 |