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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197427Generated: November 2, 2026

Toluene → Ethyl 2-chloro-5-sulfamoylthiophene-3-carboxylate

https://huagongshe.com/reaction/1197427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2-Chloro-5-sulfamoylthiophene-3-carboxylic acidHCID 1201498—
CatalystSulfuric AcidHCID 1118—
SolventEthanolHCID 702—
ProductEthyl 2-chloro-5-sulfamoylthiophene-3-carboxylateHCID 19106450—

Reaction Steps

To a round bottom flask were added 5-chloro-4-carboxythiophene-2-sulfonamide (5.0 g, 20.7 mmole) along with toluene (25 mL), ethanol (20 ml), and conc. H2SO4 (25 drops). The reaction mixture was refluxed for 96 hours. The reaction mixture was cooled and the solvent was removed under vacuum. The residue was then poured onto ice and the pH adjusted to ~8.0 using 10% sodium carbonate. The basic aqueous layer was extracted with ethyl acetate and the organic layer was washed with water, brine, and dried (MgSO4). Solvent removal yielded 3.92 g (70%) of an off white solid which was used as is: mp =98°-99° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05276025
Source datasetuspto-grants-1994_01
ORD IDord-8077273d383c4c3991829319258dbb7d
Source noteuspto-grants-1994_01