関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Acetyl chloride | HCID 6367 | — |
| 反応物 | Dimethyl 1,4-cyclohexanedicarboxylate | HCID 7198 | — |
| 反応物 | Diisopropylamine | HCID 7912 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | HCID 22421025 | HCID 22421025 | — |
反応手順
Di-isopropylamine (44.7 ml) was dissolved in dry tetrahydrofuran (400 ml) and cooled to -78° C. under nitrogen with mechanical stirring. A solution of B-butyllithium in hexane (1.6M, 197 ml) was added. After stirring at -78° C. for 10 minutes a solution of dimethyl cyclohexane-1,4-dicarboxylate (56.6 g, Lancaster) in tetrahydrofuran (200 ml) was added. After stirring for a further 30 minutes at -78° C. a solution of acetyl chloride (22.5 ml) in tetrahydrofuran (200 ml) was added. The reaction mixture was allowed to warm up to room temperature over a period of 3 hours. Water was then added and the mixture extracted with ether. The ethereal extracts were washed with water, saturated sodium bicarbonate solution, dilute hydrochloric acid and brine, and then were dried over anhydrous magnesium sulphate. Evaporation under reduced pressure gave a colourless oil which was slowly distilled to yield dimethyl 1-acetylcyclohexane-1,4-dicarboxylate (23.3 g, b.pt. 114°-120 C. at 0.4 mmHg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05466710 |
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| 出典データセット | uspto-grants-1995_11 |
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| ORD ID | ord-7a01cc761f6a426c93cc4b606233d47c |
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| 出典メモ | uspto-grants-1995_11 |
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