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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266591Generated: October 30, 2026

Acetic Acid → 4-(N,N-dimethylsulphamoyl)-2-trifluoromethylbenzoic acid

https://huagongshe.com/reaction/266591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSulfuric AcidHCID 1118—
ReactantIsoamyl NitriteHCID 8053—
ReactantHCID 54168288HCID 54168288—
SolventWaterHCID 962—
Product4-(N,N-dimethylsulphamoyl)-2-trifluoromethylbenzoic acidHCID 54115067—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 4-(N,N-dimethylsulphamoyl)-2-trifluoromethylbenzamide (1.38 g), acetic acid (10 ml) and concentrated sulphuric acid (0.5 ml) were heated to 70° C. and isoamyl nitrite (15 ml) was added over 4 hours. After cooling the mixture was poured into water and extracted with ethyl acetate and washed with water. The organic phase was extracted with 2M sodium carbonate and the aqueous layer acidified to pH 1 with 2M HCl. This was extracted with ethyl acetate, washed with water, dried (anhydrous magnesium sulphate) and filtered. The filtrate was evaporated to dryness and the residue passed through a short silica column eluting with dichloromethane-ethyl acetate to give 4-(N,N-dimethylsulphamoyl)-2-trifluoromethylbenzoic acid (0.98 g) as a white solid, m.p. 188.8°-189.4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650533
Source datasetuspto-grants-1997_07
ORD IDord-36572f42a4e246f7a2fee2369c55acd2
Source noteuspto-grants-1997_07