참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Benzene, (1-methylenepropyl)- | HCID 74871 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 촉매 | Titanium(2+);dichloride | HCID 10290777 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | Sec-Butylbenzene | HCID 8680 | 42% |
반응 단계
(1R,7S)-1,3,10,10-Tetramethyltricyclo-[5.2.1 .02,6 ]-deca-2,5-dienyl)(η5 -cyclopentadienyl)titanium dichloride (21 mg, 0.05 mmol, prepared as in Example 6) together with 2-phenyl-1-butene (132 mg, 1 mmol) and freshly distilled toluene (5 ml) were placed into a 50 ml round-bottomed flask. After degassing with three freeze/thaw cycles the vessel was filled with hydrogen (3 evacuate/refill cycles). n-Butyllithium (0.2 ml, 22.5 M, 0.5 mmol) was then added via syringe at room temperature and the resulting dark grey/green reaction mixture was stirred under a pressure of 20 p.s.i. hydrogen, while excluding light, for 40 hours. The hydrogen pressure was vented and the reaction vessel opened to air. Aqueous hydrochloric acid (2 ml, 5 M) was added and mixture was stirred for 5 minutes. The organic phase was separated and the aqueous phase extracted with ether (3×5 ml). The combined organic phases were dried (sodium sulphate) and the solvents removed iii vacuo to provide 2-phenylbutane (56 mg, 0.42 mmol) of 10.3% ee (assessed using gas chromatography, Astec α-DA column, 65° C.).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05929266 |
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| 출처 데이터셋 | uspto-grants-1999_07 |
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| ORD ID | ord-11d64296e4c2474b8b19a06bbc3bc0d9 |
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| 출처 메모 | uspto-grants-1999_07 |
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