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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894929Generated: October 29, 2026

1,2-Dichloroethane → 5-(2-Cyano-4-trifluoromethylphenoxy)-2-nitrobenzoic acid

https://huagongshe.com/reaction/894929

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantSulfuric AcidHCID 1118—
ReactantPotassium NitrateHCID 24434—
Reactant3-(2-Cyano-4-trifluoromethylphenoxy)benzoic acidHCID 13013684—
SolventWaterHCID 962—
Product5-(2-Cyano-4-trifluoromethylphenoxy)-2-nitrobenzoic acidHCID 13013685—

Reaction Conditions

Temperature0 °C

Reaction Steps

The product from (a) (9.22 g) was added in portions to a mixture of 1,2-dichloroethane (25 ml) and concentrated sulphuric acid (40 ml) stirred at 0° C. Potassium nitrate (3.13 g) was then added in portions with stirring at 0° C., over a period of 15 minutes. The mixture was then stirred at 0° C. for 30 minutes, allowed to warm to room temperature, and poured into 200 ml of ice and water. The mixture was stirred until the ice had melted, and filtered with suction. The solid which separated on evaporation of the dichloroethane was washed with water and taken up in ether. The ether solution was treated with charcoal, dried and petroleum (b.p. 40°-60° C.) added. The solid which separated was identified as the required benzoic acid derivative (7.8 g) having a melting point of 190°-192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04285723
Source datasetuspto-grants-1981_08
ORD IDord-911f047edde345b1851bb80170794e69
Source noteuspto-grants-1981_08