참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phthalic Anhydride | HCID 6811 | — |
| 반응물 | 2-Cyclohexen-1-one | HCID 13594 | — |
| 반응물 | Tributylphosphine | HCID 13831 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | 3-Butylcyclohexanone | HCID 566193 | 53% |
반응 단계
To 30 ml of anhydrous diethyl ether were added 3.8 g (20 mmol) of cuprous iodide and 4.0 g (20 mmol) of tri-n-butylphosphine, and the mixture was stirred for about 1 hour at room temperature in an atmosphere of nitrogen and then cooled to -78° C. Then, 25.6 ml (40 mmol) of a 15 % by weight hexane solution of n-butyllithium was added, and the mixture was stirred for 30 minutes, and 1.92 g (20 mmol) of 2-cyclohexenone was added. The mixture was further stirred for 1 hour at -78° C. Then, 5 ml of hexamethylphosphoric tiramide was added, and the mixture was stirred for about 10 minutes. Phthalic anhydride (2.96 g, 20 mmol) was further added, and the mixture was stirred for 3 hours at room temperature. After the reaction, a solution of 4 g (100 mmol) of sodium hydroxide in 50 ml of water was added, and the mixture was stirred for about 1 hour. It was extracted with ether, washed, and dried to afford 6.22 g of a crude product. The crude product was distilled to afford 1.62 g (10.5 mmol) of 3-n-butylcyclohexanone in a yield of 53%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04009196 |
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| 출처 데이터셋 | uspto-grants-1977_02 |
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| ORD ID | ord-02cc188640d848deaa2c2349341f38ee |
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| 출처 메모 | uspto-grants-1977_02 |
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