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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053585Generated: October 26, 2026

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

https://huagongshe.com/reaction/2053585

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Phenoxybenzyl chlorideHCID 93291—
Reactantcis-4,5-Diphenylimidazolidine-2-thioneHCID 45258634—
SolventEthanolHCID 702—
Product2-[(3-Phenoxybenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole HydrochlorideHCID 6856951994.1%

Reaction Steps

A mixture of intermediate 25 (200 mg, 0.786 mmol) and 3-phenoxybenzyl chloride (343 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 350 mg of the product 241. 1H NMR (DMSO-d6) δ 11.25 (s, 2H), 7.55-7.30 (m, 6H), 7.30-7.25 (m, 1H), 7.25-7.10 9m, 1H), 7.15-6.90 (m, 6H), 6.90-6.70 (m, 4H), 5.79 (s, 2H), 4.81 (s, 2H); MS: m/z 437 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326792B2
Source datasetuspto-grants-2008_02
ORD IDord-dcc6d5a66da5465280033bd0043af99a
Source noteuspto-grants-2008_02