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HRID 18756Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/18756

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,4-Dichlorobenzyl chlorideHCID 7609—
Eduktcis-4,5-Diphenylimidazolidine-2-thioneHCID 45258634—
LösungsmittelEthanolHCID 702—
Produkt2-[(3,4-Dichlorobenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole HydrochlorideHCID 6856816261,5%

Reaktionsschritte

A mixture of intermediate 25 (200 mg, 0.786 mmol) and 3,4-dichlorobenzyl chloride (0.218 mL, 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 217 mg of the product 204. 1H NMR (DMSO-d6) δ 11.40 (s, 2 H), 7.95 (d, 1 H), 7.78 (d, 1 H), 7.65 (d, 1 H), 7.20-6.90 (m, 6 H), 6.90-6.60 (m, 4 H), 5.78 (s, 2 H), 4.85 (s, 2 H); MS: m/z 413 (M++1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741493B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-15dc94b02c864acabbe6a3689896919b
Quellennotizuspto-grants-2010_06