Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871865Generated: October 30, 2026

Hydrochloric Acid → 2-(Difluoromethoxy)-4-fluoro-1-nitrobenzene

https://huagongshe.com/reaction/871865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant5-Fluoro-2-nitrophenolHCID 9937—
ReactantSodium CarbonateHCID 10340—
ReactantSodium chlorodifluoroacetateHCID 2734985—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product2-(Difluoromethoxy)-4-fluoro-1-nitrobenzeneHCID 4631158889%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3.14 g (20.0 mmol) 5-fluoro-2-nitrophenol in 36 mL of DMF are added 6.1 g (40.0 mmol) of sodium chlorodifluoroacetate and 3.31 g (24.0 mmol) of powdered sodium carbonate. The reaction mixture is heated at 100°C. for 4 hours 30 minutes and is then allowed to cool to room temperature. Aqueous 4N HCl solution is added and the mixture is stirred at room temperature for 2 hours. The resulting mixture is diluted with 100 mL of water and 100 mL of ether. The aqueous phase is extracted with ether and the organic phases are then combined, washed with aqueous 1N NaOH solution and then with saturated aqueous NaCl, dried over Na2SO4, filtered and concentrated under vacuum. 3.68 g of the expected product are obtained in the form of a yellow oil, which is used as obtained in the following step. Yield=89%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975250B2
Source datasetuspto-grants-2015_03
ORD IDord-42073bb1e22b4f65a9a404d9ac4a6e70
Source noteuspto-grants-2015_03