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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831548Generated: October 25, 2026

Water → 2-Benzyloxy-4-(2-chloro-4-difluoromethoxy-phenyl)-3-nitro-pyridine

https://huagongshe.com/reaction/1831548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant(2-Chloro-4-(difluoromethoxy)phenyl)boronic acidHCID 22052056—
Reactant2-(Benzyloxy)-4-chloro-3-nitropyridineHCID 22052065—
CatalystHCID 178418476HCID 178418476—
SolventWater 1,2-dimethoxyethaneHCID 18180031—
Product2-Benzyloxy-4-(2-chloro-4-difluoromethoxy-phenyl)-3-nitro-pyridineHCID 2205204768%

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) (6.59 g, 24.9 mmol) in DME/H2O, was added 2-chloro-4-difluoromethoxy-phenylboronic acid (Wilde, et al. WO 99/01454) (5.54 g, 24.9 mmol), Ba(OH)2 8H2O (7.86 g, 24.9 mmol), and Pd(PPh3)2Cl2 (1.01 g, 1.45 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 to give 6.9 g (68%) of 2-benzyloxy-4-(2-chloro-4-difluoromethoxy-phenyl)-3-nitro-pyridine as a viscous oil; MS(AP) m/z 408.9 [(M+H)+, 100].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067658B2
Source datasetuspto-grants-2006_06
ORD IDord-fd79df0ca8cf4f239cb05b304b695031
Source noteuspto-grants-2006_06