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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 126703Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/126703

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPropargyl bromideHCID 7842—
Edukt1,1-DibromoethaneHCID 11201—
EduktAmmonium ChlorideHCID 25517—
Edukt2-Pentanone, 5-chloro-HCID 79993—
EduktMagnesiumHCID 5462224—
LösungsmittelDiethyl EtherHCID 3283—
Produkt7-Chloro-4-hydroxy-4-methyl-1-heptyneHCID 12898739—

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04254036
Quelldatensatzuspto-grants-1981_03
ORD IDord-6df25f8fcda442fa8959ab015a89da1c
Quellennotizuspto-grants-1981_03