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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 464027Erstellt: 24. Oktober 2026

p-Bromochlorobenzene → 1-Chloro-4-(2-propyn-1-yl)benzene

https://huagongshe.com/de/reaction/464027

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-BromochlorobenzeneHCID 7806—
Edukt1-Methoxypropa-1,2-dieneHCID 139403—
EduktMagnesiumHCID 5462224—
Katalysatorcopper(I) bromideHCID 24593—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1-Chloro-4-(2-propyn-1-yl)benzeneHCID 13660255—

Reaktionsschritte

Place 59 g (2.43 mole) of magnesium turnings into a four-neck flask equipped with mechanical stirrer under N2 atmosphere. Add 500 ml of anhydrous ether and then add a solution of 465 g (2.43 mole) of 1-bromo-4-chlorobenzene in 1000 ml of anhydrous ether dropwise while stirring. Stir one hour after the completion of addition. Transfer and add this Grignard reagent to a solution of 170 g (2.43 mole) of 1-methoxy-1,2-propanediene and 69 g of copper (I) bromide in 300 ml of anhydrous ether with cooling. Stir for another ten minutes after the completion of addition. Add saturated aqueous solution of ammonium hydroxide and decant ether solution. Wash the solid residue with ether (3×50 ml). Wash the combined ether solutions with 1N HCl, saturated aqueous sodium bicarbonate, and with H2O. Dry over magnesium sulfate, evaporate, and distill in vacuo to yield the title compound, b.p. 99°-105° C. (15 mmHg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04545995
Quelldatensatzuspto-grants-1985_10
ORD IDord-9fb62b8a79e4438f98e0f3f914fc6c04
Quellennotizuspto-grants-1985_10