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HRID 377135作成日:2026年10月27日

Allyl chloride → 3-Butenylbenzene

https://huagongshe.com/reaction/377135

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl chlorideHCID 7850—
反応物ChlorobenzeneHCID 7964—
反応物SodiumHCID 5360545—
反応物HCID 178507079HCID 178507079—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物3-ButenylbenzeneHCID 1303372.2%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06024897
出典データセットuspto-grants-2000_02
ORD IDord-d9ab18159501461daa378d8761e23012
出典メモuspto-grants-2000_02