Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276936Generated: October 31, 2026

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

https://huagongshe.com/reaction/2276936

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 1N 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 numberUS09133145B2
Source datasetuspto-grants-2015_09
ORD IDord-f3691eda11bd41ff98e41dd4645d098d
Source noteuspto-grants-2015_09