関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bromocyclopentane | HCID 8728 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Propanedioic acid, dibutyl ester | HCID 136925 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Di-n-butyl cyclopentylmalonate | HCID 18380099 | 23.5% |
反応手順
A 0.5-liter three-neck flask equipped with a stirrer was purged with nitrogen gas, and 7.2 g (0.3mols) of sodium hydride and 250 ml of dewatered tetrahydrofuran were put thereinto in a nitrogen stream atmosphere. With stirring, the mixture was cooled to 0° C., and, while its temperature was kept cooled, 66 ml (0.3 mols) of di-n-butyl malonate was dropwise added thereto over a period of 30 minutes. After the addition, the mixture was heated up to room temperature, and 32 ml of cyclopentyl bromide was dropwise added thereto, and refluxed for 5 hours. After this was cooled to room temperature, 10 g of sodium hydride and 32 ml of cyclopentyl bromide were added thereto, and refluxed further for 8 hours. The resulting reaction mixture was washed with 200 ml of water, and subjected to distillation under reduced pressure to obtain 20 g of di-n-butyl cyclopentylmalonate. The yield was 23.5%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06204215B1 |
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| 出典データセット | uspto-grants-2001_03 |
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| ORD ID | ord-c7c9b2bf62cc46faada2c78aa4f5a96e |
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| 出典メモ | uspto-grants-2001_03 |
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