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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765067Generated: October 30, 2026

Benzyl Bromide → 3-(Benzyloxy)-2-bromopyridine

https://huagongshe.com/reaction/1765067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-3-pyridinolHCID 23070—
SolventDimethylformamideHCID 6228—
Product3-(Benzyloxy)-2-bromopyridineHCID 1077800094.1%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 2-bromo-pyridine-3-ol (50.4 g, 0.29 mol), benzyl bromide (45.5 g, 0.28 mol) and potassium carbonate (52 g, 0.38 mol) in dry N,N-dimethylformamide (DMF; 300 mL) was heated at 110° C. for 30 minutes. The mixture was filtered through a pad of Celite®, the solvent was removed under reduced pressure and the black residue was taken up between ice cold 0.5 M aqueous NaOH and EtOAc. The organic phase was washed twice with brine, dried (MgSO4), and concentrated under reduced pressure to yield 69.6 g (93%) of the title compound as a brown oil. HRMS m/z calcd for C12H10BrNO (M)+ 263.9946. found 263.9939. *Previously described in J. Med. Chem. 1996, 39, 5267–5275.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226925B2
Source datasetuspto-grants-2007_06
ORD IDord-06e32383508c4278bfe889de86205fd4
Source noteuspto-grants-2007_06