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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1789455Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1789455

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-BromochlorobenzeneHCID 7806—
EduktAmmonium ChlorideHCID 25517—
Edukt1-Methoxypropa-1,2-dieneHCID 139403—
EduktMagnesiumHCID 5462224—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelN-[4-(1-Hydroxy-2-(1H-imidazol-1-yl)ethyl]phenyl]methanesulfonamideHCID 13763390—
Produkt1-Chloro-4-(2-propyn-1-yl)benzeneHCID 13660255—

Reaktionsschritte

In a flask containing 59 g (2.43 mole) magnesium turnings in 500 ml anhydrous ether under an atmosphere of nitroge add slowly a solution of 465 g (2.43 mole) of 4-bromochlorobenzene in 1 liter 4 anhydrous ether. With caution, once the Grignard has started maintain slow reflux until all 4-bromochlorobenzene has been added. Stir an additional hour and then add this Grignard (maintain slow reflux) to a suspension of 170 g (2.43 mole) methoxyallene and 69 g of cuprous bromide in 300 ml anhydrous ether under N2. When addition is complete, stir another 10 minutes and then add saturated ammonium chloride. Decant off the ether solution wash the solid residue with ether (3×50 ml). Combine the ether extracts and wash with lN HCl, saturated aqueous sodium bicarbonate, water and dry over magnesium sulfate. Evaporate off the ether and distill the residue in vacuo to obtain the title compound (99-105 mmHg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04689341
Quelldatensatzuspto-grants-1987_08
ORD IDord-ba9c9b48fdb74de58d6c82f059e70a26
Quellennotizuspto-grants-1987_08