참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | 1-Isocyanato-4-methoxybenzene | HCID 79443 | — |
| 반응물 | (+)-Styrene oxide | HCID 114705 | — |
| 촉매 | Lithium Chloride | HCID 433294 | — |
| 생성물 | (5R)-3-(4-methoxyphenyl)-5-phenyl-2-oxazolidinone | HCID 53894593 | 53.8% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05624600 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-533bfd7a4c5d4057b5b495e5fffe3c3b |
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| 출처 메모 | uspto-grants-1997_04 |
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