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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 461461Erstellt: 26. Oktober 2026

Sodium hydride → 1-[2,4-Dichloro-beta-(2-thienylmethoxy)phenethyl]imidazole hydrochloride

https://huagongshe.com/reaction/461461

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt(+-)-alpha-(2,4-Dichlorophenyl)-1H-imidazole-1-ethanolHCID 32238—
Edukt2-(Chloromethyl)thiopheneHCID 69830—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-[2,4-Dichloro-beta-(2-thienylmethoxy)phenethyl]imidazole hydrochlorideHCID 2139392655,7%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A solution of 1-(2,4-dichloro-phenyl)-2-(1-imidazolyl) ethanol (1.5 g, 5.8mmole) dissolved in dry tetrahydrofuran (10 ml) was added to a stirred suspension of sodium hydride (0.39 g, as 80% dispersion in oil, 16 mmole) in dry tetrahydrofuran (10 ml) and warmed to 70° C for 90 minutes. The mixture was cooled in ice and a solution of 2-chloromethyl-thiophene (1.16 g, 8.8 mmole) in dry tetrahydrofuran was added. The mixture was heated at 70° for 3 hours and allowed to stir at room temperature overnight. The solvent was removed under vacuum and the residue stirred with dry ether (200 ml). The ether solution was filtered through celite and saturated with hydrogen chloride gas to precipitate an oil which was solidified by trituration with ether and ethylacetate. The solid product was collected and recrystallized from a mixture of acetone and di-isopropyl ether to give 1-[2,4-dichloro-β-(2-thienylmethoxy)phenethyl]imidazole hydrochloride as fine white crystals (0.63 g, 31%) m.p. 153°-154° C. (Found: C, 49.2; H, 3.8; N, 7.3. C16H14Cl2N2OS.HCl requires C, 49.3; H, 3.9; N, 7.2%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04062966
Quelldatensatzuspto-grants-1977_12
ORD IDord-9d7474e7f621458da5add39693f6cf87
Quellennotizuspto-grants-1977_12