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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22986Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/22986

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt1-Methoxypropa-1,2-dieneHCID 139403—
EduktMagnesiumHCID 5462224—
Edukt4,4-Dimethyl-8-iodochromanHCID 22592649—
Katalysator1,1-DibromoethaneHCID 11201—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelDiethyl EtherHCID 3283—
Produkt3-(4,4-Dimethylchroman-8-yl)1-propyneHCID 22592634—

Reaktionsbedingungen

Temperatur35 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06849658B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-ab5e059495be4757aa7d64eb183652b4
Quellennotizuspto-grants-2005_02