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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903592Generated: October 26, 2026

Iodine → p-Chloroprenylbenzene

https://huagongshe.com/reaction/1903592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantEthyl BromideHCID 6332—
Reactantp-BromochlorobenzeneHCID 7806—
Reactant1-Chloro-3-methyl-2-buteneHCID 10429—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Productp-ChloroprenylbenzeneHCID 31646064%

Reaction Conditions

Temperature20 °C

Reaction Steps

Under nitrogen atmosphere, 55.1 g of magnesium turnings, 800 ml of tetrahydrofuran, and about 0.1 g of several pieces of iodine were put in a flask. With stirring, 2 ml of ethyl bromide was added, whereupon coloration by iodine disappeared. Then, a solution of 361.7 g of p-bromochlorobenzene in 2 liters of tetrahydrofuran was added dropwise at such a speed that the reaction temperature was maintained at 25° C. to 30° C. After the addition, the mixture was further stirred for 1 hour, and cooled to about 20° C. A solution of 256.8 g of prenyl chloride in 800 ml of tetrahydrofuran was added dropwise at 15° C. to 20° C. over the course of about 4 hours. After the addition, the mixture was left to stand overnight at room temperature. Two liters of a 10% by weight aqueous solution of ammonium chloride were added, and the mixture was separated into an organic layer and an aqueous layer. The aqueous layer was extracted with 300 ml of diethyl ether. The diethyl ether layer was combined with the organic layer previously separated, and washed with water, dried, concentrated, and distilled to give 218.3 g (yield 64.0%) of p-chloroprenylbenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04436939
Source datasetuspto-grants-1984_03
ORD IDord-e845d51c3bf74f8088a6672306956ca5
Source noteuspto-grants-1984_03