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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377135Generated: October 25, 2026

Allyl chloride → 3-Butenylbenzene

https://huagongshe.com/reaction/377135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
ReactantChlorobenzeneHCID 7964—
ReactantSodiumHCID 5360545—
ReactantHCID 178507079HCID 178507079—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product3-ButenylbenzeneHCID 1303372.2%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06024897
Source datasetuspto-grants-2000_02
ORD IDord-d9ab18159501461daa378d8761e23012
Source noteuspto-grants-2000_02