Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361429Generated: October 30, 2026

Diethanolamine → N,N-Bis-(2-hydroxy-ethyl)-2-nitrobenzenesulfonamide

https://huagongshe.com/reaction/1361429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethanolamineHCID 8113—
ReactantTriethylamineHCID 8471—
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
SolventDichloromethaneHCID 6344—
ProductN,N-Bis-(2-hydroxy-ethyl)-2-nitrobenzenesulfonamideHCID 60723400—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-nitrobenzenesulfonyl chloride (10.5 g, 47.6 mmol) in anhydrous methylene chloride (25 mL) was added dropwise with stirring to a 0° C. solution of diethanolamine (5.00 g, 47.6 mmol) and triethylamine (4.92 g, 47.6 mmol) in anhydrous methylene chloride (50 mL). Reaction stirred three hours at 0° C. and then overnight at room temperature. Reaction mixture concentrated under reduced pressure. Residue dissolved in ethyl acetate, washed with 1 N NaOH, saturated NaHCO3, and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by normal phase HPLC on a Biotage pre-packed silica gel column eluting with ethyl acetate to afford the title compound. MS(ESI) m/z 291 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880001B2
Source datasetuspto-grants-2011_02
ORD IDord-301e39da6e614b9b9a4334aa92c782ee
Source noteuspto-grants-2011_02