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Tetrahydrofuran → 1-(Diphenylmethyl)azetidin-3-yl methanesulfonate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | Dibenzylazetidin-3-ol | HCID 131731899 | — |
| 生成物 | 1-(Diphenylmethyl)azetidin-3-yl methanesulfonate | HCID 2758716 | 92% |
反応手順
To a solution of dibenzylazetidin-3-ol (500 mg, 2.09 mmol) in THF (21 mL) at 0° C. under nitrogen was added methanesulfonyl chloride (194 μL, 2.51 mmol) and triethylamine (612 μL, 4.39 mmol). The reaction mixture was stirred for 1 h then concentrated to dryness. The residue was dissolved in dichloromethane, washed with water and brine. The organic layer was dried over Na2SO4, filtered and concentrated to dryness to give the title product (0.61 g, 92%) as a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08846711B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-61c31edeb8ca44868d045b53dca99afb |
| 出典メモ | uspto-grants-2014_09 |