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HRID 1277748作成日:2026年10月25日

Propargyl bromide → 7-Chloro-4-hydroxy-4-methyl-1-heptyne

https://huagongshe.com/reaction/1277748

反応式

関与物質

役割名称HCID仕込み量
反応物Propargyl bromideHCID 7842—
反応物1,1-DibromoethaneHCID 11201—
反応物Ammonium ChlorideHCID 25517—
反応物2-Pentanone, 5-chloro-HCID 79993—
反応物MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
生成物7-Chloro-4-hydroxy-4-methyl-1-heptyneHCID 12898739—

反応条件

温度-5 °C

反応手順

To a mixture of 6.69 g. of magnesium in 20 ml. of ether under argon, is added 0.1 g. of mercuric chloride and 0.1 g. of dibromoethane. The mixture is stirred for 10 minutes and 0.5 ml. of propargyl bromide is added. A 50 ml. portion of ether is added, followed by a solution of 30 g. of 5-chloro-2-pentanone and 32.55 g. of propargyl bromide in 45 ml. of ether with stirring, at a rate to maintain vigorous reflux. The mixture is stirred an additional 15 minutes, cooled to -5° C. and an ice cold saturated solution of ammonium chloride is added dropwise. The ether layer is decanted and filtered. The solids are washed with ether which is also filtered. The combined ether filtrates are washed with water, dried over magnesium sulfate and the solvent removed giving the product as an orange oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04278806
出典データセットuspto-grants-1981_07
ORD IDord-feb9c3078a82453f828db91e0537fd1e
出典メモuspto-grants-1981_07