Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867967Generated: October 26, 2026

Triethylamine → Triethylammonium 2-mercaptobenzenesulfonate

https://huagongshe.com/reaction/867967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAnilinium 2-mercaptobenzenesulfonateHCID 21289555—
ProductTriethylammonium 2-mercaptobenzenesulfonateHCID 2128956350.3%

Reaction Steps

Then, 2.0 g of the resulting anilinium 2-mercaptobenzenesulfonate was subjected to ion-exchange column chromatography (about 30 ml of Dowex 50W-X2, 100-200 mesh, H-form was filled into a column) and eluted with a mixed solvent of methanol and water (4/1, v/v). Acidic fractions were concentrated under reduced pressure, and about 50 ml of isopropanol was added to the resulting syrup. The solvent was evaporated under reduced pressure. To 1.1 g of the resulting syrup, about 4 ml of isopropanol was added to form a solution. Triethylamine (0.58 g) was added to the solution, and the resulting crystals were collected by filtration to give 0.84 g of the captioned compound as colorless crystals (melting point: 89° to 90° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04777267
Source datasetuspto-grants-1988_10
ORD IDord-748b44393511451da0101d6c8f5f41a5
Source noteuspto-grants-1988_10