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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904417Generated: October 25, 2026

Iodine → 6,6-Dimethyl-1-heptene

https://huagongshe.com/reaction/1904417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantNeopentaneHCID 10041—
ReactantHomoallyl bromideHCID 21241—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product6,6-Dimethyl-1-hepteneHCID 14459387—

Reaction Steps

A solution of 2,2-Dimethylpropane (15.1 g, 0.10 mol) in dry tetrahydrofuran (80 ml) was added dropwise to a mixture of magnesium turnings (2.43 g, 0.10 mol) in dry tetrahydrofuran (20 ml) containing a single crystal of iodine, at such a rate so as to maintain the solvent at reflux. The resulting solution was allowed to cool to room temperature and decanted from the residual magnesium under nitrogen into a fresh flask. The solution was diluted with dry tetrahydrofuran (150 ml), cooled to -20° C. under an atmosphere of nitrogen treated with cuprous bromide dimethyl sulphide complex and stirred for 20 minutes. The resulting solution was then treated with 4-bromo-1-butene (13.5 g, 0.10 mol) and stirred at -20° C. for 16 hours and then at 20° C. for 4 hours. The reaction mixture as quenched with saturated aqueous ammonium chloride solution (10 ml), diluted with ether (200 ml) and washed with an aqueous solution of ammonia (2×200 ml of 10%). The solution was dried over sodium sulfate and distilled at atmospheric pressure to yield 6,6-dimethyl- 1-heptene as a colourless oil, having a boiling point of 120°-125° C., and the following structural characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837333
Source datasetuspto-grants-1989_06
ORD IDord-bfdb595376384f2ba24e31c6ab9ed302
Source noteuspto-grants-1989_06