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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702596Generated: October 31, 2026

Tetrachlorophthalic anhydride → HCID 12852398, compound

https://huagongshe.com/reaction/1702596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrachlorophthalic anhydrideHCID 8326—
Reactant4-Aminophenyl trifluoromethyl sulphoneHCID 136315—
ProductHCID 12852398HCID 1285239856%

Reaction Steps

14 g (0.05 mol) of tetrachlorophthalic anhydride and 11 g (0.05 mol) of 4-trifluoromethylsulphonylaniline were heated to 200° C. and the mixture was kept at this temperature for 2 hours. It was then cooled and the reaction product was precipitated by adding ice-water. The product was then filtered off, washed with 50 ml of methanol and then stirred with 10% strength sodium hydroxide solution until it had dissolved. The impurities were filtered off and aqueous dilute hydrochloric acid was added to the filtrate. The crystals thereby obtained were filtered off and dried at 50° C. 14 g (that is to say 56% of theory) of N-(4-trifluoromethylsulphonylphenyl)-tetrachlorophthalamic acid of melting point 92°-97° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04348411
Source datasetuspto-grants-1982_09
ORD IDord-c691bc781c164ee7beee5b9670d7c649
Source noteuspto-grants-1982_09