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Thionyl Chloride → 5-(Chloromethyl)-2-(1H-pyrazol-1-yl)pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | (6-(1H-pyrazol-1-yl)pyridin-3-yl)methanol | HCID 15980534 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 5-(Chloromethyl)-2-(1H-pyrazol-1-yl)pyridine | HCID 16655946 | 95% |
反応手順
To a solution of alcohol (III) (10.5 g, 59.9 mmol) in CH2Cl2 (150 ml), SOCl2 (36 g, 22 ml, 299.6 mmol) was added and the resulting reaction mixture was stirred at room temperature for a period of between 12 to 18 hours. The excess SOCl2 was quenched with saturated aqueous NaHCO3. The resulting mixture was extracted with CH2Cl2 and washed with brine. Removal of solvent gave a compound of formulae (11.15 g, 95% yield) as a white solid. MS-ESI=194.06, 196.06, 1H NMR (ppm): 8.59(H3′, d), 8.43(H6, d), 8.03(H2, d), 7.89(H3, dd), 7.78(H5′, s), 6.50(H4′, t), 4.65(—CH2-).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07538225B2 |
| 出典データセット | uspto-grants-2009_05 |
| ORD ID | ord-60690913a7724bd09dfd2b0267e0b481 |
| 出典メモ | uspto-grants-2009_05 |