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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054082Generated: October 31, 2026

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

https://huagongshe.com/reaction/1054082

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-(6-Phenylpyridin-3-yl)propan-1-olHCID 67511142—
SolventAcetonitrileHCID 6342—
Product1-(6-phenylpyridin-3-yl)propyl 1H-imidazole-1-carboxylateHCID 57329870—

Reaction Steps

Synthesized using compound 44a (150 mg, 0.70 mmol), CDI (570 mg, 3.52 mmol) and acetonitrile (9 mL) according to Method E. Crude product was purified by flash chromatography on silica-gel using a mixture of hexane/ethyl acetate (3:1) as eluent. White solid. Yield: 116 mg, 54%. 1H NMR (CDCl3, 500 MHz): δH (ppm)=1.04 (t, J=7.4 Hz, 3H), 2.01-2.15 (m, 1H), 2.22 (dt, J=14.3, 7.2 Hz, 1H), 5.92 (t, J=7.1 Hz, 1H), 7.09 (dd, J=1.6, 0.6 Hz, 1H), 7.41-7.51 (m, 4H), 7.75-7.80 (m, 2H), 7.98-8.03 (m, 2H), 8.17-8.19 (m, 1H), 8.74-8.77 (m, 1H); 13C NMR (CDCl3, 125 MHz): δC (ppm)=9.8, 28.7, 79.8, 117.0, 120.3, 126.9, 128.8, 129.3, 130.8, 132.3, 135.0, 137.0, 138.6, 148.0, 148.3, 158.0; MS (ESI): m/z=308.30 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394290B2
Source datasetuspto-grants-2016_07
ORD IDord-28133a8172824305b8abcf4c9a35fe46
Source noteuspto-grants-2016_07