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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877933Generated: October 30, 2026

Tetrahydrofuran → 4-(6,7-Dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)-3-(n-propyl)benzonitrile

https://huagongshe.com/reaction/1877933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-(6,7-Dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)-3-((E)-propenyl)benzonitrileHCID 58827182—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-(6,7-Dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)-3-(n-propyl)benzonitrileHCID 58827094—

Reaction Steps

A suspension of 4-(6,7-Dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)-3-((E)-propenyl)benzonitrile (0.150 g, 0.602 mmol), 20% (w/w) palladium on carbon (0.040 g), THF (15 mL), and EtOH (15 mL) is stirred under an atmosphere of hydrogen (1 atm) for 60 h. The suspension is the filtered and the filtrate concentrated. The residue is then purified by flash chromatography (Hexane/EtOAc, and then 10% MeOH/EtOAc) to give 4-(6,7-Dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)-3-(n-propyl)benzonitrile as a white solid. MS (ESI) m/z 252.1 (M+H); 1H NMR (400 MHz, CDCl3) δ ppm 1.04 (t, J=7.3 Hz, 3 H), 1.63-1.77 (m, 2 H), 2.33-2.45 (m, 1 H), 2.62-2.80 (m, 2 H), 2.92 (app t, J=7.1 Hz, 2 H), 3.04-3.19 (m, 1 H), 5.58 (dd, J=7.8, 5.6 Hz, 1 H), 6.73 (d, J=8.1 Hz, 1 H), 6.81 (s, 1 H), 7.25 (s, 1 H), 7.41 (d, J=8.1 Hz, 1 H), 7.51 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314097B2
Source datasetuspto-grants-2012_11
ORD IDord-6dcbe196f1bd4b319ee215fb5a971f3a
Source noteuspto-grants-2012_11