関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Pyrrolidone | HCID 12025 | — |
| 反応物 | N-(2,2-Dimethoxyethyl)-2-propenamide | HCID 9898899 | — |
| 生成物 | N-[2,2-Dimethoxyethyl]-3-[2-oxopyrrolidin-1-yl]propionamide | HCID 21182207 | — |
反応手順
10 g (62.8 mmol) of the acrylamido acetal from Example 2 are mixed with 6 g (70.5 mmol) of pyrrolidone and, after addition of one drop of Triton B, the mixture is warmed to 80° C. After 10 minutes, the reaction is terminated. The thin-layer chromatogram shows no UV absorbing acetal. The product is subsequently freed from traces of solvent under a high vacuum. It is a single compound according to TLC. NMR data: 2 methylene protons at each of 2.0, 2.4, 2.5, 3.3, 3.4 and 3.6 ppm(t), 6 methoxy protons at 3.35 ppm(s), 1 acetal proton at 4.4 ppm(t), 1 amide proton at 7.2 ppm.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06265509B1 |
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| 出典データセット | uspto-grants-2001_07 |
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| ORD ID | ord-8387881e32484ec0b865b945df24520b |
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| 出典メモ | uspto-grants-2001_07 |
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