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Diethyl Malonate → 1,1-Diethyl cyclopent-3-ene-1,1-dicarboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diethyl Malonate | HCID 7761 | — |
| 反応物 | Lithium hydride | HCID 62714 | — |
| 反応物 | 1,4-Dichloro-cis-2-butene | HCID 6432115 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 1,1-Diethyl cyclopent-3-ene-1,1-dicarboxylate | HCID 10987569 | — |
反応手順
To a stirred solution of 160 g of diethyl malonate in 1.5 l of dry dimethylformamide at 0° C. under nitrogen was slowly added 30 g of lithium hydride. After the evolution of hydrogen ceased (2 hours) 143 g of cis-1,4-dichloro-2-butene was slowly added and the mixture allowed to come to room temperature. After 72 hours, the mixture was diluted with a mixture of ether and hexane (1:4) and poured into water. The organic layer was washed with water and brine before drying over magnesium sulfate. Distillation gave diethyl 3-cyclopentene-1,1-dicarboxylate, bp 70°-80° C./0.1 mm, containing a small amount (~10%) of diethyl 2-vinylcyclopropane-1,1-dicarboxylate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05011846 |
| 出典データセット | uspto-grants-1991_04 |
| ORD ID | ord-f23345d95300427987ed83da2cfa58e4 |
| 出典メモ | uspto-grants-1991_04 |