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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-(6,7-Dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)-3-((E)-propenyl)benzonitrile | HCID 58827182 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(6,7-Dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)-3-(n-propyl)benzonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314097B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-6dcbe196f1bd4b319ee215fb5a971f3a |
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| Source note | uspto-grants-2012_11 |
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