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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529480Generated: November 3, 2026

Dimethylformamide → 4-Bromopyridine-3-carbaldehyde

https://huagongshe.com/reaction/1529480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-Bromopyridinium chlorideHCID 88100—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product4-Bromopyridine-3-carbaldehydeHCID 1111674031.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A suspension of 4-bromopyridine hydrochloride (5.0 g, 25.7 mmol) in THF (100 mL) was purged with N2 and cooled to −78° C. A solution of lithium diisopropylamide (2.0 M solution in heptane/THF/ethylbenzene, 27.0 mL, 54.0 mmol) was added over 3 minutes. After 30 minutes, DMF (8.56 mL, 110.6 mmol) was added. The reaction mixture was stirred at −78° C. for 15 minutes before rapidly warming to room temperature in a water bath. The reaction was allowed to stir at ambient temperature for 18 hours. The reaction was quenched with saturated NH4Cl (100 mL) and extracted with EtOAc. The combined organic extracts were washed with water and brine, dried over Na2SO4, evaporated, and chromatographed (Analogix 150 g silica gel column eluting with a gradient of 100% heptane 50% EtOAc/heptane over 1 hour) to give 1.50 g (31%) of the title compound as a light yellow solid. MS m/z 186 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090625B2
Source datasetuspto-grants-2015_07
ORD IDord-7ac806df20da4729926b9a925aa4d1c1
Source noteuspto-grants-2015_07