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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573158Generated: October 28, 2026

1,3-Difluoro-2-nitrobenzene → Methyl 4-fluoro-2-(3-fluoro-2-nitrophenoxy)benzoate

https://huagongshe.com/reaction/573158

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Difluoro-2-nitrobenzeneHCID 87922—
ReactantMethyl 4-fluorosalicylateHCID 2775386—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-fluoro-2-(3-fluoro-2-nitrophenoxy)benzoateHCID 67227494—

Reaction Steps

To a solution of methyl 4-fluoro-2-hydroxybenzoate (1.225 g) in anhydrous tetrahydrofuran (25 mL) was added potassium t-butoxide (0.808 g). The mixture was stirred for 20 minutes at room temperature. A solution of 1,3-difluoro-2-nitrobenzene (0.955 g) in tetrahydrofuran (6 mL) was then added dropwise. The resulting mixture was stirred at room temperature for 1 hour, then at 80° C. overnight. The reaction mixture was quenched with water (40 mL) and extracted with dichloromethane. The organic solution was dried (MgSO4), filtered and concentrated. The residue was purified on a silica gel column, eluting with 25% ethyl acetate in hexane to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029404B2
Source datasetuspto-grants-2015_05
ORD IDord-d9073d7030874f248998c733b01aa736
Source noteuspto-grants-2015_05