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HRID 22986생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/22986

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물1-Methoxypropa-1,2-dieneHCID 139403—
반응물MagnesiumHCID 5462224—
반응물4,4-Dimethyl-8-iodochromanHCID 22592649—
촉매1,1-DibromoethaneHCID 11201—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Diethyl EtherHCID 3283—
생성물3-(4,4-Dimethylchroman-8-yl)1-propyneHCID 22592634—

반응 조건

온도35 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849658B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-ab5e059495be4757aa7d64eb183652b4
출처 메모uspto-grants-2005_02