戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1903592作成日:2026年10月25日

Iodine → p-Chloroprenylbenzene

https://huagongshe.com/reaction/1903592

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Ethyl BromideHCID 6332—
反応物p-BromochlorobenzeneHCID 7806—
反応物1-Chloro-3-methyl-2-buteneHCID 10429—
反応物Ammonium ChlorideHCID 25517—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物p-ChloroprenylbenzeneHCID 31646064%

反応条件

温度20 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04436939
出典データセットuspto-grants-1984_03
ORD IDord-e845d51c3bf74f8088a6672306956ca5
出典メモuspto-grants-1984_03