참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Allyl chloride | HCID 7850 | — |
| 반응물 | Chlorobenzene | HCID 7964 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | HCID 178507079 | HCID 178507079 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 3-Butenylbenzene | HCID 13033 | 72.2% |
반응 단계
In 220 g of toluene, 20.3 g (0.883 mol) of sodium dispersion was reacted with 46.5 g (0.413 mol) of chlorobenzene, to prepare phenyl sodium. The resultant toluene slurry was stirred for 2.5 hours under heat reflux. The thus-obtained black slurry was cooled, and then a toluene (40 g) solution containing 31.6 g (0.413 mol) of allyl chloride was added to the cooled slurry, keeping the reaction temperature in the range of from -10° C. to 0° C., and then the reaction mixture was allowed to stand, for aging, for 30 minutes at room temperature. After the reaction was completed, the reaction mixture was subjected to hydrolysis with 350 ml of water in the range of 5 to 20° C., and then the resultant organic layer was washed with 300 ml of water twice, according to a usual manner. Toluene was removed therefrom by atomospheric distillation, and the residual orange oil was subjected to distillation under reduced pressure in the same manner as in Example 7. As a result, 39.4 g (0.298 mol, yield 72.2%) of 4-phenyl-1-butene was given (purity 98.3%), and 6.3 g of a residue remained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06024897 |
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| 출처 데이터셋 | uspto-grants-2000_02 |
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| ORD ID | ord-d9ab18159501461daa378d8761e23012 |
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| 출처 메모 | uspto-grants-2000_02 |
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