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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231428Generated: October 31, 2026

1,2-Dichloroethane → 2-Chloro-4-fluoro-5-nitrobenzaldehyde

https://huagongshe.com/reaction/231428

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantSulfuric AcidHCID 1118—
ReactantPotassium NitrateHCID 24434—
Reactant2-Chloro-4-fluorobenzaldehydeHCID 145024—
SolventDichloromethaneHCID 6344—
Product2-Chloro-4-fluoro-5-nitrobenzaldehydeHCID 1356377564.8%

Reaction Steps

To 300 ml of 1,2-dichloroethane that had been cooled to 0° C. was added 31.3 g (0.197 mole) of 2-chloro-4-fluorobenzaldehyde, prepared by the method of Example 2, Steps A and B. Subsequently, 19.96 g (0.197 mole) of potassium nitrate was added to the reaction mixture, and dropwise addition of 300 ml of concentrated sulfuric acid followed while maintaining the temperature between 0° C. and 5° C. The reaction was complete after 80 minutes, and 750 ml of methylene chloride was added to the reaction mixture. The phases were separated, and the sulfuric acid phase was extracted three times with 150 ml of methylene chloride. The extracts were combined with the organic phase before being washed three times with 450 ml of water. The extracts were dried over anhydrous magnesium sulfate, filtered, and the solvent was evaporated under reduced pressure, leaving an amber oil weighing 32.5 g as a residue. This oil was passed through a column of silica gel, eluting with ethyl acetate/heptane (1/4). The appropriate fractions were combined, and the solvent was evaporated under reduced pressure, leaving 26.0 g of 2-chloro-4-fluoro-5-nitrobenzaldehyde as an amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04846882
Source datasetuspto-grants-1989_07
ORD IDord-b6796875862347e59c359609be31541d
Source noteuspto-grants-1989_07