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Triethylamine → (S)-1-Benzyl-3-mesyloxypyrrolidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | (S)-(-)-1-Benzyl-3-pyrrolidinol | HCID 2733875 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | (S)-1-Benzyl-3-mesyloxypyrrolidine | HCID 10934081 | 98% |
反応手順
(S)-1-Benzyl-3-hydroxypyrrolidine (1003.5 g, 5.66 mol) was dissolved in toluene (12 L) and the solution stirred and cooled to 0°-5° C. Triethylamine (680 g, 6.67 mol) was added followed by methanesulfonyl chloride (760 g, 6.63 mol) over a 4 hour period. A slurry formed after 30 minutes. The mixture was allowed to stir an additional 1.5 hours and 7% sodium bicarbonate (12 L) was added to the reaction mixture and the organic layer separated. The aqueous layer was extracted with toluene (4 L and 2 L) and the combined organic layers washed with saturated sodium bicarbonate (3×6 L), dried over MgSO4 and concentrated under reduced pressure to give (S)-1-benzyl-3-mesyloxypyrrolidine as a yellow oil (1.41 kg, 98%):
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05466828 |
| 出典データセット | uspto-grants-1995_11 |
| ORD ID | ord-598cb616651a47af9cf13705182b4fa2 |
| 出典メモ | uspto-grants-1995_11 |