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(Diethylamino)sulfur trifluoride → tert-Butyl(4S,5R)-4-(fluoromethyl)-2,2-dimethyl-5-[4-(fluoromethylthio)phenyl]-1,3-oxazolidine-3-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | tert-Butyl(4S,5R)-4-(fluoromethyl)-2,2-dimethyl-5-[4-(methylsulfinyl)phenyl]-1,3-oxazolidine-3-carboxylate | HCID 68720168 | — |
| 触媒 | Antimony trichloride | HCID 24814 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | tert-Butyl(4S,5R)-4-(fluoromethyl)-2,2-dimethyl-5-[4-(fluoromethylthio)phenyl]-1,3-oxazolidine-3-carboxylate | HCID 68719639 | 86.5% |
反応手順
A solution of diethylamino sulfurtrifluoride (DAST), (9.34 g, 1.75 eq ) in 10 ml of dichloromethane was added drop wise to the solution of 14 (12.3 g) and antimony (III) chloride (0.23 g, 0.03 eq ) in 150 ml of dichloromethane (anhydrous) at −5° C., and the reaction mixture was warmed up to room temperature overnight. A cold saturated solution of sodium bicarbonate (80 ml) was added and stirred for 30 min and extracted with dichloromethane (100 ml×2). The organic layer was washed with a 10% solution of sodium bicarbonate and with brine (50 ml) and dried over sodium sulfate. After purification, via a column, 10.7 g of the desired product (as a heavy oil) was obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07361689B2 |
| 出典データセット | uspto-grants-2008_04 |
| ORD ID | ord-ebb033e654d74be2a94b18917bab6ff1 |
| 出典メモ | uspto-grants-2008_04 |