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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | 3-(2-Cyano-4-trifluoromethylphenoxy)benzoic acid | HCID 13013684 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(2-Cyano-4-trifluoromethylphenoxy)-2-nitrobenzoic acid | HCID 13013685 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04285723 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-911f047edde345b1851bb80170794e69 |
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| Source note | uspto-grants-1981_08 |
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