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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583076Generated: October 30, 2026

Water → 2-Fluoro-6-nitrobenzaldehyde

https://huagongshe.com/reaction/583076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
Reactant4-Fluoro-2-nitrotolueneHCID 67965—
ReactantDimethylformamide dimethyl acetalHCID 78373—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-6-nitrobenzaldehydeHCID 13524043—

Reaction Conditions

Temperature140 °C

Reaction Steps

To a solution of 4-fluoro-2-nitrotoluene (3 g, 17.96 mmol) in DMF (25 ml) was added (MeO)2CHNMe2 (3.12 ml, 23.35 mmol) and the mixture warmed at 140° C. for 4 hours in argon atmosphere. Then the solution was allowed to reach room temperature and diethyl ether (100 ml) and water (100 ml) was added. The organic layer was washed with water (2×100 ml) and brine (1×100 ml), dried (MgSO4) and solvent concentrated at reduced pressure, affording an oil which was treated with NaIO4 (11.5 g, 53.6 mmol). The mixture was stirred in 50% aqueous THF (100 ml) at room temperature for 24 hours. The mixture was filtered in a celite pad and eluted with EtOAc. The organic layer was washed with NaHCO3 (saturated solution, 3×100 ml), dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography (50% CH2Cl2 /Hexane) affording 2-nitro-6-fluorobenzaldehyde as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929072
Source datasetuspto-grants-1999_07
ORD IDord-c149d81fc02d45d287d562b2fee18e6c
Source noteuspto-grants-1999_07