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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370844Generated: October 27, 2026

Benzyl Bromide → Ethyl 5-(benzyloxy)-6-chloronicotinate

https://huagongshe.com/reaction/2370844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 6-chloro-5-hydroxynicotinateHCID 86687988—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductEthyl 5-(benzyloxy)-6-chloronicotinateHCID 86687989—

Reaction Steps

To a stirred mixture of ethyl 6-chloro-5-hydroxynicotinate (2 g, 0.01 mol) in Toluene (50.0 mL) were added K2CO3 (2.76 g, 0.02 mol, Rankem, India) and benzyl bromide (2 g, 0.0012 mol). The reaction mixture was stirred for 2 h at room temperature. After completion of the reaction (monitored by TLC, 20% EtOAc in hexane), the reaction mixture was quenched with water (50 mL), extracted with EtOAc (50 mL×3). The combined organic layers were dried over anhydrous sodium sulfate and purified by column chromatography, silica gel (60-120 mesh) using 12-16% EtOAc in petroleum ether as the eluent to give the title compound. MS (ESI, positive ion) m/z: 292.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710043B2
Source datasetuspto-grants-2014_04
ORD IDord-2b8147f373db4c2a87897ae18c2a1579
Source noteuspto-grants-2014_04