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2,6-Lutidine → 3,3,3-Trifluoropropyl trifluoromethanesulfonate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2,6-Lutidine | HCID 7937 | — |
| 反応物 | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| 反応物 | 3,3,3-Trifluoro-1-propanol | HCID 137512 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3,3,3-Trifluoropropyl trifluoromethanesulfonate | HCID 14132849 | — |
反応手順
To a cold (−25° C.), stirred solution of 2,6-lutidine (18.38 mL, 158 mmol) in CH2Cl2 (120 mL) was added Tf2O (24.88 mL, 147 mmol) over 3 min, and stirred for 5 min. To the reaction mixture was added 3,3,3-trifluoropropan-1-ol (12 g, 105 mmol) over an interval of 3 min. After 2 hr, the reaction mixture was warmed to room temperature and stirred for 1 hr. The reaction mixture was concentrated to half volume, then purified by loading directly on silica gel column (330 g ISCO) and eluted with CH2Cl2. Obtained Preparation 1M (13.74 g, 53%) as a colorless oil. 1H NMR (400 MHz, CDCl3) δ ppm 4.71 (2H, t, J=6.15 Hz), 2.49-2.86 (2H, m).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08822454B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-9b193238fec8414dbb1c1a46e35a7a20 |
| 出典メモ | uspto-grants-2014_09 |