참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenothiazine | HCID 7108 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Acryloyl chloride | HCID 13140 | — |
| 반응물 | 5-(Hydroxymethyl)oxazolidin-2-one | HCID 10290773 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-Acryloyloxymethyl-oxazolidin-2-one | HCID 18934230 | — |
반응 단계
105 g (0.90 mol.) of 5-hydroxymethyl-oxazolidin-2-one were placed into a one liter, three necked, round bottomed flask equipped with a paddle stirrer and thermometer. This was followed by 500 ml of tetrahydrofuran, 101 g (1.0 mol.) of triethylamine and 0.5 g of phenothiazine. Stirring was started as 90 g (1.0 mol.) of acryloyl chloride were added dropwise in such a way that the contents of the flask were maintained at 30° C. or less. When the addition was complete, the contents were stirred overnight at room temperature. The triethylamine hydrochloride was filtered and the solution was allowed to stand over NaHCO3 and Na2SO4. The solution was filtered, transferred to a one liter, round bottomed flask and placed on a rotoevaporator. The solution was concentrated by purging with a stream of air while rotating the flask. The resulting liquid was confirmed by 13C NMR to contain a mixture of the desired product and unreacted starting material.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05733648 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-77519deec78d44d89cdc131b10b54df8 |
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| 출처 메모 | uspto-grants-1998_03 |
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