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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413828Generated: October 25, 2026

Iodine → HCID 20467612, compound

https://huagongshe.com/reaction/1413828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Butene, 1-bromo-3-methyl-HCID 70092—
Reactant2-(4-Bromophenyl)-2-methyl-1,3-dioxolaneHCID 614920—
ReactantMagnesiumHCID 5462224—
Catalyst1,2-DibromoethaneHCID 7839—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20467612HCID 2046761277.7%

Reaction Steps

To a mixture of 10.2 g of magnesium turnigns, 300 ml of tetrahydrofuran and a few pieces of iodine, was added 3.8 g of 1,2-dibromoethane with stirring under a stream of nitrogen. Additionally, a solution of 93.0 g of 2-(p-bromophenyl)-2-methyl-1,3-dioxolane dissolved in 300 ml of tetrahydrofuran was dropped while keeping the temperature at 50°-55° C. After dropping, the reaction mixture was stirred for 30 minutes, and cooled to room temperature. A solution of 66.0 g of prenyl bromide in 100 ml of tetrahydrofuran was then dropped to the reaction mixture while keeping the reaction temperature at 50°-55° C., which was allowed to stand for overnight at room temperature. A solution of 20 g of ammonium chloride in 50 ml of water was added. The organic layer was decanted, concentrated and dissolved in ethyl ether. The ethereal solution was washed with water, dried, concentrated and distilled to give 69.1 g of 2-methyl-2-(p-prenylphenyl)-1,3-dioxolane, b.p. 106-107 °C/0.10 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251543
Source datasetuspto-grants-1981_02
ORD IDord-175386732090443583e4b034005d4669
Source noteuspto-grants-1981_02