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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860473Generated: October 26, 2026

Benzyl Bromide → 5-[(Benzyloxy)carbonyl]nicotinic acid

https://huagongshe.com/reaction/860473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant3,5-Pyridinedicarboxylic acidHCID 10366—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product5-[(Benzyloxy)carbonyl]nicotinic acidHCID 5744454423.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 60% sodium hydride (527 mg) in dimethylformamide (20 mL) was added 3,5-pyridinedicarboxylic acid (2.00 g) under ice-water cooling and the mixture was stirred at 0° C. for 1 hour. To the mixture was added (bromomethyl)benzene (2.05 g) and the mixture was stirred at 60° C. for 2 hours. The mixture was partitioned between ethyl acetate and water. The organic layer was washed with water and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was triturated with ethyl acetate to give 5-[(benzyloxy)carbonyl]nicotinic acid as a pale yellow powder (722 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153854B2
Source datasetuspto-grants-2006_12
ORD IDord-73d806606503471c8e06e8a873b009fc
Source noteuspto-grants-2006_12