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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293263Generated: October 30, 2026

Water → Methyl 5-chloro-2-[(5-nitropyridin-2-yl)oxy]benzoate

https://huagongshe.com/reaction/1293263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzoic acid, 5-chloro-2-hydroxy-, methyl esterHCID 77684—
Reactant2-Chloro-5-nitropyridineHCID 78308—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-chloro-2-[(5-nitropyridin-2-yl)oxy]benzoateHCID 6942057597.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of methyl 5-chloro-2-hydroxybenzoate (2.35 g, 12.6 mmol), 2-chloro-5-nitropyridine (2.00 g, 12.6 mmol), and potassium carbonate (5.23 g, 37.8 mmol) in N,N-dimethylformamide (50 mL) was stirred at 120° C. for 1 h. The reaction mixture was poured into water and the aqueous mixture was extracted with a mixture (3/1) of ethyl acetate and toluene. The organic extracts were washed with brine, dried over sodium sulfate, and concentrated. The residue was purified by flush column chromatography on silica gel eluting with hexane/ethyl acetate (4/1) to afford 3.79 g (97%) of the title compound: 1H-NMR (CDCl3) δ 8.94 (1H, d, J=2.8 Hz), 8.52 (1H, dd, J=9.0, 2.8 Hz), 8.05 (1H, d, J=2.8 Hz), 7.60 (1H, dd, J=8.6, 2.8 Hz), 7.18 (1H, d, J=8.6 Hz), 7.14 (1H, d, J=9.0 Hz), 3.73 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238714B2
Source datasetuspto-grants-2007_07
ORD IDord-a752656d7886463cbb336d2b117cc078
Source noteuspto-grants-2007_07