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Isobutyraldehyde → 1-Methyl-2-(2,2-dimethyl-2-formylethyl)-3-isopropenylcyclopent-1-ene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Isobutyraldehyde | HCID 6561 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 2-(Chloromethyl)-1-methyl-3-(prop-1-en-2-yl)cyclopent-1-ene | HCID 14217877 | — |
| 触媒 | Tetrabutylammonium Iodide | HCID 67553 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 1-Methyl-2-(2,2-dimethyl-2-formylethyl)-3-isopropenylcyclopent-1-ene | HCID 5014262 | 76% |
反応手順
A mixture of 857 g (5 moles) of 1-methyl-2-chloromethyl-3-isopropenylcyclopentene and 360 g (5 moles) of isobutyraldehyde was added in the course of 5 hours, whilst stirring, to a mixture of 480 g of 50% strength sodium hydroxide solution, 24 g of tetrabutylammonium iodide and 500 ml of toluene, at 80° C. The organic phase was then separated off and washed repeatedly with 200 ml portions of water, the toluene was stripped off and the residue was distilled in a rotary evaporator; boiling point 75°-77° C/0.3 mm Hg; nD25 : 1.4788; the structure was confirmed by the nuclear resonance spectrum; yield: 76%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04069258 |
| 出典データセット | uspto-grants-1978_01 |
| ORD ID | ord-d7319b60639041a6abb927bc89f83f0f |
| 出典メモ | uspto-grants-1978_01 |