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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754926Generated: October 28, 2026

Triethylamine → HCID 66817509, compound

https://huagongshe.com/reaction/1754926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-BromoethanolHCID 10898—
Reactant3-EthylanilineHCID 11475—
ReactantChlorosulfonyl isocyanateHCID 70918—
SolventDichloromethaneHCID 6344—
ProductHCID 66817509HCID 6681750980%

Reaction Steps

2-Bromoethanol (0.28 mL, 4.00 mmol) was added to a solution of chlorosulfonyl isocyanate (0.35 mL, 4.00 mmol) in dichloromethane (1.8 mL) at 0° C. After stirring for 90 minutes, a solution of 3-ethylaniline (0.55 mL, 4.40 mmol) and triethylamine (1.23 mL, 8.80 mmol) in dichloromethane (3.6 mL) was added. The mixture was stirred for 90 minutes and then quenched with a 2 N aqueous hydrochloric acid solution. The mixed solution was separated, and the aqueous layer was then extracted with ether. The organic layers were combined and washed with water and saturated brine, and then dried over sodium sulfate and concentrated under reduced pressure. The resulting residue was washed with ether (5 mL) to give 2-oxo-oxazolidine-3-sulfonic acid (3-ethylphenyl)amide (LCMS yield 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-c30b0c58ff994b0e833ae724771c3cf9
Source noteuspto-grants-2015_10