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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019755Generated: November 1, 2026

Methanol → 1-Chloro-2-fluoro-4-methoxy-5-nitrobenzene

https://huagongshe.com/reaction/1019755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
Reactant1-Chloro-2,4-difluoro-5-nitrobenzeneHCID 73867—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTolueneHCID 1140—
Product1-Chloro-2-fluoro-4-methoxy-5-nitrobenzeneHCID 5340328952%

Reaction Steps

To a suspension of potassium tert-butoxide (15.07 g, 134.3 mmol) in toluene (100 mL), and the appropriate alcohol, in this case methanol (3.80 g, 118.7 mmol), was added at 0° C. and stirred for 15 minutes. A solution of the appropriate 1-substituted 2,4-difluoro-5-nitrobenzene, in this case 1-chloro-2,4-difluoro-5-nitrobenzene (20.0 g, 103.3 mmol), in toluene (50 mL) was added at 0° C. and stirred for 5 hours at room temperature. Water (1000 mL) was added and the mixture was extracted with EtOAc (3×100 mL). The combined organic extracts were washed with water (150 mL), brine (150 mL), dried (Na2SO4) and concentrated under reduced pressure. The crude residue was purified by column chromatography on neutral silica gel using 5-10% EtOAc in hexane to give the title compound (11.0 g, 52%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716287B2
Source datasetuspto-grants-2014_05
ORD IDord-03b81957356b46d3ac7b10cdf0ba4e2d
Source noteuspto-grants-2014_05