HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463961Generated: October 31, 2026
Hydrochloric Acid → HCID 13560012, compound
https://huagongshe.com/reaction/463961
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | Ethyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-aminobenzoate hydrochloride | HCID 20249654 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13560012 | HCID 13560012 | — |
Reaction Steps
Ethyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-aminobenzoate hydrochloride (12 g) and conc. hydrochloric acid (6.6 ml) were added to acetic acid (85 ml), and the resultant mixture was cooled to less than 10° C. A solution of sodium nitrite (2.5 g) in water (6 ml) was dropwise added thereto. When the resulting mixture became completely transparent, benzene (20 ml), acetic acid (20 ml) saturated with sulfur dioxide and copper chloride (1.5 g) were added thereto. After stirring overnight, the reaction mixture was poured onto ice-water. The deposited oily substance was extracted with chloroform, washed with water and dried over anhydrous magnesium sulfate. The extract was concentrated and allowed to stand. The crystallized substance was recrystallized from hexane to give 9 g of 4-(2-chloro-4-trifluoromethylphenoxy)-2-ethoxycarbonylbenzenesulfonyl chloride. M.P., 96°-96.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04545812 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-1cfd7b754f5947f3b90760328921deeb |
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| Source note | uspto-grants-1985_10 |
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