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Pyridine → 2-adamantyl Chloroformate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | 2-Adamantanol | HCID 64149 | — |
| 反応物 | Triphosgene | HCID 94429 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-adamantyl Chloroformate | HCID 10878537 | — |
反応手順
To a stirred solution of 2-adamantanol (0.912 g, 6 mmol) in dry CH2Cl2 (15 mL) was added bis(trichloromethyl)carbonate (0.653 g), pyridine in dry CH2Cl2 (10 mL) at 0° C. The reaction mixture was warmed to room temperature and stirred for two hours. The solvent was removed in vacuo at 30° C., taken up in ethyl acetate (30 mL) and stirred for 10 minutes. The pyridinium hydrochloride precipitate was filtered off and the solvent removed in vacuo at 30° C., to give an oil which solidified upon standing (1.29 g, 100%). IR (film) 1778 cm-1 ; NMR (CDCl3) δ1.55-1.65 (2H, m), 1.70-1.80 (4H, m), 1.85-1.95 (4H, m), 2.00-2.10 (2H, m), 2.15-2.20 (2H, m), 5.02 (1H, 6, J 3.3 Hz CHOCOCl).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05622983 |
| 出典データセット | uspto-grants-1997_04 |
| ORD ID | ord-3c7f7a3c2a4b43a6adae20c471b2d13a |
| 出典メモ | uspto-grants-1997_04 |