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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18839Generated: October 24, 2026

Triethylamine → 2-(Methylthio)-cis-4,5-diphenyl-4,5-dihydro-imidazole-1-carboxylic Acid Phenyl Ester

https://huagongshe.com/en/reaction/18839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
Reactantcis-4,5-Diphenyl-2-methylthio-4,5-dihydro-1H-imidazole hydroiodideHCID 68569083—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-(Methylthio)-cis-4,5-diphenyl-4,5-dihydro-imidazole-1-carboxylic Acid Phenyl EsterHCID 5965545959.2%

Reaction Steps

To a solution of 2-(methylthio)-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole hydroiodide (42) (1.00 mg, 2.52 mmol), triethylamine (0.528 mL, 0.379 mmol), 4-dimethylamino-pyridine (10 mg) in dichloromethane (20 mL) is added phenyl chloroformate (0.379 mL, 3.02 mmol), and the mixture is stirred at rt overnight. The reaction mixture is diluted with dichloromethane and washed with water, brine, and the organic layer is dried (MgSO4), filtered, and evaporated. The residue is purified by chromatography on silica gel; gradient elution with heptane:EtOAc (70:30-60:40) gives 0.58 g of the product 548. 1H NMR (CDCl3) δ 7.25-6.95 (m, 11H), 6.95-6.80 (m, 2H), 6.80-6.70 (m, 2H), 5.80-5.65 (m, 2H), 2.62 (s, 3H). MS: m/z 389 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741493B2
Source datasetuspto-grants-2010_06
ORD IDord-38f7a9f155714a62b76115b2a7142ad9
Source noteuspto-grants-2010_06