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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054084Generated: November 1, 2026

1,1'-Carbonyldiimidazole → 1-(6-phenylpyridin-3-yl)ethyl 1H-imidazole-1-carboxylate

https://huagongshe.com/reaction/1054084

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-(6-Phenylpyridin-3-yl)ethanolHCID 67509895—
SolventAcetonitrileHCID 6342—
Product1-(6-phenylpyridin-3-yl)ethyl 1H-imidazole-1-carboxylateHCID 57329871—

Reaction Steps

Synthesized using compound 45a (170 mg, 0.85 mmol), CDI (692 mg, 4.27 mmol) and acetonitrile (10 mL) according to Method E. Crude product was purified by flash chromatography on silica-gel using a mixture of hexane/ethyl acetate (2:1) as eluent. White solid. Yield: 107 mg, 43%. 1H NMR (CDCl3, 500 MHz): δH (ppm)=1.82 (d, J=6.9 Hz, 3H), 6.16 (q, J=6.6 Hz, 1H), 7.08 (dd, J=1.7, 0.8 Hz, 1H), 7.41-7.53 (m, 4H), 7.76-7.85 (m, 2H), 7.98-8.03 (m, 2H), 8.17 (d, J=1.3 Hz, 1H), 8.78 (d, J=1.9 Hz, 1H); 13C NMR (CDCl3, 125 MHz): δC (ppm)=21.5, 74.9, 117.1, 120.4, 126.9, 128.8, 129.3, 130.8, 133.3, 134.7, 137.0, 138.6, 147.9, 148.0, 158.0; MS (ESI): m/z=294.28 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394290B2
Source datasetuspto-grants-2016_07
ORD IDord-b565c7e7bc71401da6984210156f8bc4
Source noteuspto-grants-2016_07