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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1380344Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1380344

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 nitrogen, and 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 1N 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
PatentnummerUS04581370
Quelldatensatzuspto-grants-1986_04
ORD IDord-4aa74c6da4be459394e1d919e2ca96a0
Quellennotizuspto-grants-1986_04