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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463961Generated: October 31, 2026

Hydrochloric Acid → HCID 13560012, compound

https://huagongshe.com/reaction/463961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
ReactantEthyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-aminobenzoate hydrochlorideHCID 20249654—
ReactantSodium NitriteHCID 23668193—
CatalystCupric ChlorideHCID 24014—
SolventAcetic AcidHCID 176—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductHCID 13560012HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04545812
Source datasetuspto-grants-1985_10
ORD IDord-1cfd7b754f5947f3b90760328921deeb
Source noteuspto-grants-1985_10