참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 2-(4-Methoxyphenyl)oxirane | HCID 98048 | — |
| 반응물 | Lithium Chloride | HCID 433294 | — |
| 반응물 | 4-Butylphenyl isocyanate | HCID 2796313 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-(4-Butylphenyl)-5-(4-methoxyphenyl)-2-oxazolidinone | HCID 19956702 | 14.5% |
반응 단계
In a 20 ml-three necked flask, 0.013 g of lithium chloride and 3.8 ml of DMF were placed. To the mixture, a solution of 1.09 g (6.22 mM) of 4-butylphenyl isocyanate and 6.20 mM of optically active 4-methoxystyrene oxide in 1.3 ml of DMF was added dropwise in 12 minutes under refluxing and stirring in nitrogen atmosphere, followed by refluxing for 50 minutes under stirring. After the reaction, the reaction mixture was left standing for cooling, then poured into water, and subjected to extraction with ethyl acetate. The organic layer was washed with water, dried with anhydrous sodium sulfate and evaporated under reduced pressure to obtain a residue The residue was purified by silica gel column chromatography (eluent: toluene/ethyl acetate=10/1) and recrystallized from methanol to obtain 0.29 g of optically active 3-(4-butylphenyl)-5-(4-methoxyphenyl)-2-oxazolidinone (Yield: 14.5%).
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-911e781ae40e4f81bc059adeb5bc3892 |
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| 출처 메모 | uspto-grants-1997_04 |
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