関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | 1-Isocyanato-4-methoxybenzene | HCID 79443 | — |
| 反応物 | (+)-Styrene oxide | HCID 114705 | — |
| 触媒 | Lithium Chloride | HCID 433294 | — |
| 生成物 | (5R)-3-(4-methoxyphenyl)-5-phenyl-2-oxazolidinone | HCID 53894593 | 53.8% |
反応手順
3.50 g (29.1 mM) of (R)-(+)-styrene oxide, 0.035 g of lithium chloride and 14 ml of N,N-dimethylformamide (DMF) were placed in a 50 ml-three necked flask. Under refluxing and stirring in nitrogen atmosphere, a solution of 4.38 g (29.4 mM) of 4-methoxyphenyl isocyanate in 3.5 ml of DMF was added dropwise to the mixture in 40 minutes, followed by refluxing for 40 minutes under stirring. After the reaction, the reaction mixture was poured into ice water to precipitate a crystal. The crystal was recovered by filtration, washed with water and recrystallized from methanol. The resultant crystal was purified by silica gel column chromatography (eluent: toluene/ethyl acetate =100/1) and recrystallized from a toluene/methanol mixture solvent to obtain 4.22 g of (5R)-3-(4-methoxyphenyl)-5-phenyl-2-oxazolidinone (Yield: 53.8%). This compound showed the following phase transition series.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05624600 |
|---|
| 出典データセット | uspto-grants-1997_04 |
|---|
| ORD ID | ord-533bfd7a4c5d4057b5b495e5fffe3c3b |
|---|
| 出典メモ | uspto-grants-1997_04 |
|---|