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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831504Generated: November 2, 2026

Water → 2-(Benzyloxy)-4-(2,4-dichlorophenyl)-3-nitropyridine

https://huagongshe.com/reaction/1831504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant(2,4-Dichlorophenyl)boronic acidHCID 2734659—
Reactant2-(Benzyloxy)-4-chloro-3-nitropyridineHCID 22052065—
CatalystHCID 178418476HCID 178418476—
SolventWater 1,2-dimethoxyethaneHCID 18180031—
Product2-(Benzyloxy)-4-(2,4-dichlorophenyl)-3-nitropyridineHCID 2205212882%

Reaction Steps

To a solution of 2-benzyloxy-4-chloro-3-nitro-pyridine (Wilde, et. al. WO 99/01454, which is incorporated herein by reference)(5 g, 18.9 mmol) in DME/H2O, was added 2,4-dichlorophenylboronic acid (3.60 g, 18.9 mmol), Ba(OH)2 0.8H2O (5.96 g, 18.9 mmol), and Pd(PPh3)2Cl2 (0.77 g, 1.09 mmol) and the mixture was heated at reflux for 5 h. The reaction was cooled and poured into EtOAc and H2O (500 mL). The EtOAc layer was washed with H2O, brine, dried (Na2SO4), filtered and concentrated in vacuo. Purification using flash chromatography (10% EtOAc-Hexane) gave 5.79 g (82%) of 2-benzyloxy-4-(2,4-dichloro-phenyl)-3-nitro-pyridine as a viscous oil: crude MS (AP) m/z 375.2 [(M+H)+, 100].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067658B2
Source datasetuspto-grants-2006_06
ORD IDord-08f37e7bfc5e4dfd89b42ba44dc1aca4
Source noteuspto-grants-2006_06