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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51296Generated: October 26, 2026

1-Bromopropane → 1-Propyl-1H-imidazole-4-carbaldehyde

https://huagongshe.com/reaction/51296

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopropaneHCID 7840—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant18-Crown-6HCID 28557—
Reactant1H-Imidazole-4-carbaldehydeHCID 76428—
SolventTetrahydrofuranHCID 8028—
Product1-Propyl-1H-imidazole-4-carbaldehydeHCID 1035176647%

Reaction Steps

Imidazole-4-carboxaldehyde (30 g, 0.31 mol) was added portionwise to a solution of sodium hydride (13.9 g, 60% dispersion in mineral oil, 0.348 mol) in tetrahydrofuran (450 ml), and the solution was stirred for 45 minutes. n-Propyl bromide (31.2 ml, 0.344 mol) was then added portionwise, followed by 18-crown-6 (150 mg), and the mixture was heated under reflux for 18 hours. Aqueous ammonium chloride solution was added to the cooled solution, and the mixture was extracted with ethyl acetate (2×) and dichloromethane (2×). The combined organic extracts were dried (MgSO4), filtered, and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel, eluting with ethyl acetate: pentane (40:60), to give the title compound, 20.2 g, 47% yield. 1H-NMR (DMSO-d6, 400 MHz) δ: 0.80 (t, 3H), 1.76 (m, 2H), 3.98 (t, 2H), 7.84 (s, 1H), 8.04 (s, 1H), 9.70 (s, 1H). LRMS: m/z (TSP+) 277.3 [2M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713496B2
Source datasetuspto-grants-2004_03
ORD IDord-81713f3831ec431895fbb267489a2c43
Source noteuspto-grants-2004_03