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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7409Generated: October 28, 2026

Dimethylformamide → 1-(4-phenylbutyl)-1H-imidazole-2-carboxamide

https://huagongshe.com/reaction/7409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(4-phenylbutyl)-1H-imidazoleHCID 21990225—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-(4-phenylbutyl)-1H-imidazole-2-carboxamideHCID 21990243—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Reaction under N2 atmosphere. A mixture of DIPA (0.455 mol) in THF (500 ml) was stirred at −78° C. Butyllithium, 2.5M/hexane (0.390 mol) was added dropwise at −40° C. The mixture was stirred for 15 min, then re-cooled to −78° C. A solution of 1-(4-phenylbutyl)-1H-imidazole, prepared according to the procedure described in J. Chem. Soc., Perkin Trans., 1 (1975), 17, 1670–1671, (0.325 mol) in THF (350 ml) was added dropwise at −60° C. The mixture was stirred for one hour, then re-cooled to −78° C. This mixture was added dropwise to a mixture of N,N-dimethylformamide (0.390 mol, dry, p.a.) in THF (500 ml), stirred at −78° C. The reaction mixture was stirred for one hour at −78° C., then allowed to warm to room temperature while stirring overnight. A saturated aqueous NH4Cl solution (400 ml) was added and this mixture was extracted with THF. The separated organic layer was dried, filtered and the solvent evaporated, yielding 74.2 g of 1-(4-phenylbutyl)-1H-imidazole-2-carboxamide (interm. 18).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087595B2
Source datasetuspto-grants-2006_08
ORD IDord-696b82fd9a0a4806818870df0e9948e3
Source noteuspto-grants-2006_08