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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871856Generated: October 30, 2026

Methyl iodide → 1,5-Difluoro-3-methoxy-2-nitrobenzene

https://huagongshe.com/reaction/871856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3,5-Trifluoro-2-nitrobenzeneHCID 67567—
SolventAcetoneHCID 180—
Product1,5-Difluoro-3-methoxy-2-nitrobenzeneHCID 1033012995%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 2.45 g (14.0 mmol) of 1,3,5-trifluoro-2-nitrobenzene in acetone are successively added 2.9 g (21.0 mmol) of K2CO3 powder and 3.5 mL (56.0 mmol) of methyl iodide. The reaction mixture is heated at 50°C. for 2 hours and then filtered and evaporated to dryness. The residue is taken up in ethyl acetate and washed with water and with saturated aqueous NaCl solution. The organic phase is dried over Na2SO4, filtered and concentrated under vacuum. 2.52 g of the expected product are recovered in the form of a yellow solid, which is used as obtained in the following step. Yield=95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975250B2
Source datasetuspto-grants-2015_03
ORD IDord-9bc0aa9bb43c41db873da6befeb00ae8
Source noteuspto-grants-2015_03