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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220253Generated: October 31, 2026

Dimethylformamide → 6-(2-Methylphenyl)pyridine-3-carbaldehyde

https://huagongshe.com/reaction/2220253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTetrahydrofuranHCID 8028—
ReactantHexaneHCID 8058—
ReactantButyllithiumHCID 178418339—
Product6-(2-Methylphenyl)pyridine-3-carbaldehydeHCID 2472966291%

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a stirred solution of 125 mg of the above compound (0.50 mmol) in THF (2.0 mL) under argon at −74° C. was added 220 μL of nBuLi solution in hexane (2.5 M, 0.55 mmol, 1.1 eq) over 5 min, the temperature not allowed to rise above −71° C. A light green solution formed, which became dark green after 30 min. After 45 min, 49.4 μL (0.61 mmol, 1.2 eq) of DMF was added and the reaction allowed to warm to −40° C. After 14 h, a bright orange solution had formed. The reaction was quenched with 10% citric acid and the mixture stirred rapidly for 20 min at room temperature. The resulting bright yellow solution was extracted twice with EtOAc. The organic extracts were combined, dried over MgSO4, filtered and concentrated to give a yellow oil. The crude mixture thus obtained was purified by silica gel chromatography using ethyl acetate/dichloromethane (1:24) as eluant, (2.5×10 cm column), to give white solid, mp 82-84° C., 90.3 mg, 91% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417028B2
Source datasetuspto-grants-2008_08
ORD IDord-c3e589a009be4295a7a3fe85ebd0ba7a
Source noteuspto-grants-2008_08