Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250617Generated: October 25, 2026

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

https://huagongshe.com/reaction/2250617

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 numberUS07317009B2
Source datasetuspto-grants-2008_01
ORD IDord-7bc9d0b6d129489a9d9f02a62ec13d38
Source noteuspto-grants-2008_01