Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613827Generated: November 1, 2026

Water → HCID 54566916, compound

https://huagongshe.com/reaction/1613827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantChlorosulfamic acidHCID 24499—
ReactantHCID 21114759HCID 21114759—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 54566916HCID 5456691644%

Reaction Steps

To a suspension of 25.0 g (0.13 mole) of resorcinol-bis(β-hydroxyethyl)ether (Lancaster Synthesis, Windham, NH 03087) in 150 ml of acetonitrile was added simultaneously 170 ml (0.53 mole) of sulfamoyl chloride solution (3.14M solution in acetonitrile) and 54.1 g (0.54 mole) of triethylamine (temperature ≤15° C.) and the reaction mixture was stirred at ambient temperature overnight. The reaction mixture was treated with 200 ml of water and 300 ml of ethyl acetate, the layers were separated, and the organic layer was washed with two 200 ml portions of water. The organic solvents were evaporated under reduced pressure and the solid residue was treated with 500 ml of ethyl acetate and 200 ml of water. The mixture was filtered1 and the filtrate layers were separated. The organic layer was washed with five 200 ml portions of water (filtrate pH neutral to pH paper) and dried (magnesium sulfate). The solvent was evaporated under reduced pressure and the solid residue was dissolved in 300 ml of ethyl acetate and filtered through celite. The filtrate was evaporated under reduced pressure and the solid residue was recrystallized from ethyl acetate to yield 19.6 g (44%) of an off-white solid, mp 147°-149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194446
Source datasetuspto-grants-1993_03
ORD IDord-230b38eb1e2649ae8e77ca0790f8e5b7
Source noteuspto-grants-1993_03