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HRID 22986作成日:2026年10月25日

Ammonium Chloride → 3-(4,4-Dimethylchroman-8-yl)1-propyne

https://huagongshe.com/reaction/22986

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物1-Methoxypropa-1,2-dieneHCID 139403—
反応物MagnesiumHCID 5462224—
反応物4,4-Dimethyl-8-iodochromanHCID 22592649—
触媒1,1-DibromoethaneHCID 11201—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒Diethyl EtherHCID 3283—
生成物3-(4,4-Dimethylchroman-8-yl)1-propyneHCID 22592634—

反応条件

温度35 °C

反応手順

280 mg (11.5 mmol) of magnesium, activated with 1 drop of dibromoethane, are introduced into a three-necked flask under argon. A solution of 3.00 g (10.4 mmol) of 4,4-dimethyl-8-iodochroman in 15 ml of ethyl ether is added dropwise, so as to maintain the reflux of the solvent, and the reaction mixture is stirred at 35° C. for 15 minutes. It is subsequently cooled to −5° C., 40 mg (0.2 mmol) of CuI are added and a solution composed of 1.24 g (17.7 mmol) of methoxyallene in 5 ml of ethyl ether is introduced dropwise. The mixture is stirred for one hour at −5° C., allowed to return to room temperature and stirred for two hours. The reaction mixture is poured into a saturated ammonium chloride solution and extracted with ethyl acetate and the organic phase is separated by settling, dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a silica column eluted with heptane. After evaporating the solvents, 1.30 g (65%) of the expected compound are collected in the form of a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06849658B2
出典データセットuspto-grants-2005_02
ORD IDord-ab5e059495be4757aa7d64eb183652b4
出典メモuspto-grants-2005_02