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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905838Generated: November 3, 2026

Potassium Carbonate → 2-(1-Methoxycarbonylethoxy)benzenesulfonamide

https://huagongshe.com/reaction/1905838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-bromopropionateHCID 95576—
Reactant2-Hydroxybenzene-1-sulfonamideHCID 637546—
SolventAcetonitrileHCID 6342—
Product2-(1-Methoxycarbonylethoxy)benzenesulfonamideHCID 22152837—

Reaction Steps

34.6 g of 2-hydroxybenzenesulfonamide and 55.3 g of potassium carbonate are added to 800 ml of acetonitrile. With efficient stirring, 33.4 g of methyl 2-bromopropionate are added dropwise over 10 minutes and the suspension is then heated for 5 hours to 45° C. After the reaction mixture has cooled, the precipitated salts are isolated and the filtrate is concentrated in vacuo. The residue is recrystallised from ethanol, affording 41.8 of 2-(1-methoxycarbonylethoxy)benzenesulfonamide with a melting point of 140°-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04648899
Source datasetuspto-grants-1987_03
ORD IDord-bc9f9ea14d3f41908a0db240e36891de
Source noteuspto-grants-1987_03