Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288779Generated: November 1, 2026

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

https://huagongshe.com/reaction/1288779

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 numberUS05747424
Source datasetuspto-grants-1998_05
ORD IDord-7beeb2cf2e404b88b0f4f4e3929bfa54
Source noteuspto-grants-1998_05