関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 2-Oxazolidinone, 4-phenyl-, (4S)- | HCID 730424 | — |
| 反応物 | (E)-pent-2-enoyl chloride | HCID 5706546 | — |
| 反応物 | Sodium hexamethyidisilazane | HCID 45051731 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (S,E)-3-(pent-2-enoyl)-4-phenyloxazolidin-2-one | HCID 11096863 | 28.7% |
反応手順
(S)-(+)-4-Phenyl-2-oxazolidinone (4.0 g, 24 mmol, Aldrich) was dissolved in dry THF (40 mL), and the solution was cooled to -50° C. and flushed with N2. Sodium hexamethyldisilazane (1.0M in THF, 25 mL, 25 mmol) was added slowly with stirring. The compound from step 7a (2.9 g, 24 mmol) was added slowly while maintaining the temperature at -50° C., and the mixture was stirred at this temperature for 1.5 hour. The mixture was allowed to warm to 0° C. and stirred for 1 hour. Saturated aqueous NH4Cl solution was added, the mixture was stirred for 10 minutes and the mixture was extracted with methylene chloride. The extract was dried over Na2SO4, filtered and the solvent was removed. The residue was chromatographed on silica gel, eluting with 2% methanol/methylene chloride, and the product was rechromatographed with 0.5% methanol/methylene chloride to give the title compound (1.69 g). MS m/ z 246 (M+H)+, 263 (M+NH4)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05618949 |
|---|
| 出典データセット | uspto-grants-1997_04 |
|---|
| ORD ID | ord-54fbe7df9da8436eb7d74aeb74befc5f |
|---|
| 出典メモ | uspto-grants-1997_04 |
|---|