참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Iodooctane | HCID 12380 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | (5R)-3-(4-hydroxyphenyl)-5-phenyl-2-oxazolidinone | HCID 54314065 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (5R)-3-(4-octyloxyphenyl)-5-phenyl-2-oxazolidinone | HCID 53637929 | 30.1% |
반응 단계
Then, 0.30 g (1.18 mM) of (5R)-3-(4-hydroxyphenyl)-5-phenyl-2-oxazolidinone and 4.6 ml of DMF were placed in 30 ml-round bottomed flask, followed by stirring to form a solution. To the solution, 0.053 g (1.33 mM) of 60%-oily sodium hydride was added under stirring at room temperature. After the settlement of foaming, 0.25 ml (1.38 mM) of 1-iodooctane was added to the mixture, followed by stirring for 30 minutes on an oil bath kept at about 70° C. After the reaction, the reaction mixture was poured into ice water to precipitate a crystal. The crystal was recovered by filtration and washed with water, followed by purification by silica gel column chromatography (eluent: toluene/ethyl acetate =100/1) and recrystallization from a toluene-methanol mixture solvent to obtain 0.13 g of (5R)-3-(4-octyloxyphenyl)-5-phenyl-2-oxazolidinone (Yield: 30.1%).
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-ccc751841a9b4b238bdcd8e8f959367b |
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| 출처 메모 | uspto-grants-1997_04 |
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