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HRID 18766Erstellt: 24. Oktober 2026

3,4-Difluorobenzyl Chloride → 2-[(3,4-Difluorobenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole Hydrochloride

https://huagongshe.com/de/reaction/18766

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,4-Difluorobenzyl ChlorideHCID 2736954—
Eduktcis-4,5-Diphenylimidazolidine-2-thioneHCID 45258634—
LösungsmittelEthanolHCID 702—
Produkt2-[(3,4-Difluorobenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole HydrochlorideHCID 6856964363,2%

Reaktionsschritte

A mixture of intermediate 25 (200 mg, 0.786 mmol) and 3,4-difluorobenzyl chloride (0.255 mg, 1.57 mmol) in abs. EtOH (2 mL) is heated at 95° C. for 24 h. The reaction mixture is cooled to RT, evaporated to dryness, and the residue suspended in Et2O. The insoluble material is filtered to give 207 mg of the product 214. 1H NMR (DMSO-d6) δ 11.38 (s, 2 H), 7.90-7.65 (m, 1 H), 7.65-7.40 (m, 2 H), 7.20-6.90 (m, 6 H), 6.90-6.65 (m, 4 H), 5.79 (s, 2 H), 4.85 (s, 2 H); MS: m/z 381 (M++1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741493B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-8bd6e468d93f4c1da0b2c6c4a3d0a0df
Quellennotizuspto-grants-2010_06