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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255254Generated: October 26, 2026

Ethanol → (2,6-Diisopropyl-phenylsulfamoyl)-acetic acid ethyl ester

https://huagongshe.com/reaction/2255254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSulfoacetic acidHCID 31257—
ReactantDiisopropylanilineHCID 32484—
SolventDichloromethaneHCID 6344—
Product(2,6-Diisopropyl-phenylsulfamoyl)-acetic acid ethyl esterHCID 44330987—

Reaction Conditions

Temperature125 °C

Reaction Steps

Sulfoacetic acid (52 g, 371 mM) and EtOH (500 mL) were heated under reflux for 20 hours. The reaction mixture was cooled, and the excess ethanol was removed under vacuum to give 2 (see Chart I). A mixture of 2 (16.82 g, 100 mM) and POCl3 (30.67 g, 200 mM) was heated at 125° C. for 5 hours. The mixture was cooled and filtered, and excess POCl3 was removed to give 3 (see Chart I). Compound 3 (8.18 g, 43.83 mM) was added dropwise with stirring to a solution of 2,6-diisopropylaniline (15.54 g, 87.66 mM) in 50 mL CH2Cl2 maintained at 0° C. The mixture was stirred at room temperature for an additional 18 hours. The solvent was removed and the residue was redissolved in 100 mL ethyl acetate and washed with 1 N HCl and brine. The ethyl acetate was evaporated and the pure compound was isolated by chromatography over silica gel (EtOAc/hexane, 1:4 as eluant) as a white powder, 7.0 g (~50%), mp 114°-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05239082
Source datasetuspto-grants-1993_08
ORD IDord-f50c8b709851438080f600e477ebcc2b
Source noteuspto-grants-1993_08