참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Glycidol | HCID 11164 | — |
| 반응물 | 4-Aminobenzonitrile | HCID 13396 | — |
| 반응물 | Phenolate | HCID 119047 | — |
| 반응물 | 3-p-Cyanophenyl-5-methanesulfonyloxymethyloxazolidin-2-one | HCID 15281527 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | p-(N-2,3-dihydroxypropylamino)benzonitrile | HCID 10171309 | — |
반응 단계
1 Equivalent of NaH is added to a solution of 1.7 g of Na p-methoxycarbonylmethylphenoxide (obtainable by converting p-hydroxybenzyl cyanide into the corresponding carboxylic acid, esterifying with methanol to give p-methoxycarbonylmethylphenol and subsequently converting the latter into the phenoxide) in 20 ml of dimethylformamide (DMF), and the mixture is stirred at room temperature for 30 min. After that, 3.0 g of 3-p-cyanophenyl-5-methanesulfonyloxymethyloxazolidin-2-one ("A") (obtainable by reacting p-aminobenzonitrile with 2,3-epoxypropan-1-ol to give p-(N-2,3-dihydroxypropylamino)benzonitrile, reacting the latter with diethyl carbonate in the presence of K tert-butoxide to give 3-p-cyanophenyl-5-hydroxymethyloxazolidin-2-one and subsequently esterifying the latter with methanesulfone chloride), dissolved in 10 ml of DMF, are added and the mixture is once again stirred at room temperature for 15 min. Following removal of the solvent, and the customary working-up, 3-p-cyanophenyl-5-(p-methoxycarbonylmethylphenoxymethyl)oxazolidin-2-one is obtained, M.p. 114°-115°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05723480 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-db32eb67f898496ca933619d4788c566 |
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| 출처 메모 | uspto-grants-1998_03 |
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