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HRID 1904417作成日:2026年10月27日

Iodine → 6,6-Dimethyl-1-heptene

https://huagongshe.com/reaction/1904417

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物NeopentaneHCID 10041—
反応物Homoallyl bromideHCID 21241—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物6,6-Dimethyl-1-hepteneHCID 14459387—

反応手順

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:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04837333
出典データセットuspto-grants-1989_06
ORD IDord-bfdb595376384f2ba24e31c6ab9ed302
出典メモuspto-grants-1989_06