Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797167Generated: October 30, 2026

1,1'-Carbonyldiimidazole → HCID 22177242, compound

https://huagongshe.com/reaction/1797167

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 22177252HCID 22177252—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 22177242HCID 2217724231.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of N-(3,5-dichloro-phenyl)-N′-[2-(4-iodo-phenyl)-pent-4-enyl]-ethane-1,2-diamine (0.386 g, 0.81 mmol) in toluene (10 mL) was added CDI (0.18 g, 1.1 mmol, 1.4 eq). The mixture was heated to 100° C. for 16 h, then cooled to room temperature, diluted with EtOAc (25 mL) and washed twice with saturated aqueous NaCl (25 mL). The organic extracts were dried over sodium sulfate, filtered and concentrated by rotary evaporation to give a dark brown oil. The crude product was purified by flash column chromatography eluting with 10% EtOAc/hexanes to give 1-(3,5-dichloro-phenyl)-3-[2-(4-iodo-phenyl)-pent-4-enyl]-imidazolidin-2-one (0.128 g, 0.255 mmol, 30%) as a pale foam. 1H NMR (300 MHz, CDCl3): δ 7.74 (d, 2H), 7.54 (d, 2H), 7.20 (m, 3H), 5.75 (m, 1H), 5.10 (m, 2H), 3.74 (m, 3H), 3.38 (m, 2H), 3.22 (m, 1H), 3.08 (m, 1H), 2.50 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034056B2
Source datasetuspto-grants-2006_04
ORD IDord-542e32656726457ba21af3f182358482
Source noteuspto-grants-2006_04