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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824229Generated: November 1, 2026

1-Iodopropane → (E)-1-phenyl-N-(1-propylimidazol-2-yl)methanimine

https://huagongshe.com/reaction/1824229

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodopropaneHCID 33643—
Reactant(E)-N-(1H-imidazol-2-yl)-1-phenylmethanimineHCID 22147335—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(E)-1-phenyl-N-(1-propylimidazol-2-yl)methanimineHCID 2214742490%

Reaction Steps

To a solution of N-[(1E)-phenylmethylidene]-1H-imidazol-2-amine (1.00 g, 5.84 mmol) in DMF (20 mL) was added KOt-Bu (0.80 g, 7.13 mmol) and 1-iodopropane (0.63 mL, 6.46 mmol). After 3.5 h, the reaction was diluted with water (50 mL) and extracted with EtOAc (3×50 mL). The combined organic layers were washed with brine, dried over Na2SO4, decanted, and concentrated. The crude product was purified by column chromatography (Biotage, 40M) with heptanes/EtOAc (2:1) to give 1.12 g (90%) of yellow liquid: 1H NMR (400 MHz, CDCl3) δ 9.23, 7.94, 7.47, 7.02, 6.94, 4.14, 1.83, 0.95; IR (liq.) 2966, 2935, 2876, 1612, 1576, 1509, 1477, 1450, 1313, 1282, 1150, 761, 738, 716, 690 cm−1; HRMS (FAB) calcd for C13H15N3+H 214.1344, found 214.1336.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041672B2
Source datasetuspto-grants-2006_05
ORD IDord-894fc792e8c34379bd7eaeef8251d9ba
Source noteuspto-grants-2006_05