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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624335Generated: November 1, 2026

Imidazole → 1-(2-Methoxyethyl)-1H-imidazole-2-carbaldehyde

https://huagongshe.com/reaction/1624335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
ReactantTetrahydrofuranHCID 8028—
ReactantButyllithiumHCID 178418339—
Product1-(2-Methoxyethyl)-1H-imidazole-2-carbaldehydeHCID 16495065—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of the imidazole (342 mg, 2.71 mmol) in THF (3.5 mL) was cooled to −78° C. under nitrogen and n-BuLi (2.5M in hexanes, 1.4 mL, 3.5 mmol) was added. The resulting bright yellow solution was stirred at 0° C. for 10 minutes, then DMF (0.5 mL, 6.5 mmol) was added. The reaction was stirred at room temperature for 45 minutes, then was quenched by the addition of saturated aqueous NH4Cl (5 mL). The layers were separated and the aqueous solution was extracted with CH2Cl2 (10 mL×2). The organic solution was dried (Na2SO4), filtered and concentrated under reduced pressure. Purification by flash column chromatography on silica (CH2Cl2/MeOH, 32:1) gave the aldehyde as a yellow liquid (1:1 with DMF, 254 mg, 1.12 mmol, 41%). 1H NMR (CDCl3) δ 3.30 (s, 3H), 3.66 (t, 2H, J=5.1 Hz), 4.58 (t, 2H, J=5.0 Hz), 7.26 (s, 1H), 7.27 (s, 1H), 9.80 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778967B2
Source datasetuspto-grants-2014_07
ORD IDord-e6228182102048b99b4a18dbae22eb06
Source noteuspto-grants-2014_07