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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831532Generated: October 31, 2026

Ethyl Acetate → HCID 22052089, compound

https://huagongshe.com/reaction/1831532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
Reactant(4-Methoxy-2-methylphenyl)boronic acidHCID 2773486—
Reactant2-(Benzyloxy)-4-chloro-3-nitropyridineHCID 22052065—
CatalystHCID 178418476HCID 178418476—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 22052089HCID 2205208978%

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) (0.98 g, 3.7 mmol) in ethanol (10 mL) and toluene (40 mL), was added Na2CO3 (4.6 mL, 2M), 4-methoxy-2-methylphenyl boronic acid (1.0 g, 5.6 mmol), and Pd(PPh3)2Cl2 (0.156 g, 0.22 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 1.01 g (78%) of 2-benzyloxy-4-(4-methoxy-2-methyl-phenyl)-3-nitro-2,3-dihydro-pyridine as a viscous oil; MS(AP) m/z 351.6 [(M+H)+, 100], 392.0 [(M+H+CH3CN)+, 35]. The purified intermediate was used in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067658B2
Source datasetuspto-grants-2006_06
ORD IDord-39fa361049cf48e78d54ec6f0c32a526
Source noteuspto-grants-2006_06