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HRID 1764128作成日:2026年10月25日

Iodine → p-(1-Cyclooctenyl)-anisol

https://huagongshe.com/reaction/1764128

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物4-BromoanisoleHCID 7730—
反応物CyclooctanoneHCID 10403—
反応物Ammonium ChlorideHCID 25517—
反応物MagnesiumHCID 5462224—
溶媒ChloroformHCID 6212—
溶媒TetrahydrofuranHCID 8028—
生成物p-(1-Cyclooctenyl)-anisolHCID 284297—

反応条件

温度15 °C

反応手順

To a vigorously stirred suspension of 19.5 g of magnesium chips (which have been washed with chloroform and activated with iodine) in 800 ml of absolute tetrahydrofuran is added in increments a solution of 131 g of p-bromanisol in 200 ml of absolute tetrahydrofuran in such a way that it is possible to maintain gently the Crignard reaction. The reaction mixture is allowed to continue to react for 1 hour, cooled to 15° C and treated dropwise with 88 g of cyclooctanone. After the reaction mixture has been stirred for a further 5 hours, it is treated with ice and with saturated ammonium chloride solution. The whole mixture is extracted with ether, the ether layers are washed with water, dried over sodium sulphate and evaporated in vacuo. During distillation under a high vacuum, water is split off from the oily residue to thus yield the p-(1-cyclooctenyl)-anisol, which boils at 115°-118° C (0.05mm Hg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04115416
出典データセットuspto-grants-1978_09
ORD IDord-f7f504eabccd417f923fc3a2b0b66506
出典メモuspto-grants-1978_09