참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pivaloyl chloride | HCID 62493 | — |
| 반응물 | Lithium Chloride | HCID 433294 | — |
| 반응물 | 2-(Propan-2-yloxy)acetic acid | HCID 517213 | — |
| 반응물 | (S)-4-Benzyl-2-oxazolidinone | HCID 736225 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | (4S)-4-benzyl-3-(2-isopropoxyacetyl)oxazolidin-2-one | HCID 59997951 | 56.8% |
반응 단계
A solution containing 98 g of 2-isopropoxyacetic acid and 360 ml of triethylamine in tetrahydrofuran (4L) was cooled to −25° C. After 92 ml of 2,2-dimethylpropanoyl chloride was dropwise added, the reaction solution was stirred at −20° C. for 5 hours. Then, 50 g of anhydrous lithium chloride and 120 g of (4S)-4-benzyl-1,3-oxazolidin-2-one were successively added, and stirring was continued at room temperature overnight. Then, the reaction solution was filtered and evaporated. The residue was dissolved in 2 L of ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel column chromatography (elution solvent: hexane-ethyl acetate), to give 106.6 g of (4S)-4-benzyl-3-(2-isopropoxyacetyl)-1,3-oxazolidin-2-one as a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07544835B2 |
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| 출처 데이터셋 | uspto-grants-2009_06 |
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| ORD ID | ord-5178ef5a9d284d738f013980ea07e27d |
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| 출처 메모 | uspto-grants-2009_06 |
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