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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412248Generated: November 3, 2026

4-Nitrobenzenesulfonyl chloride → 4-Nitrobenzenesulfonic Acid 2-[3-(Tritylamino)phenyl]ethyl Ester

https://huagongshe.com/reaction/2412248

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzenesulfonyl chlorideHCID 7404—
ReactantDabcoHCID 9237—
ReactantSodium BicarbonateHCID 516892—
Reactant2-[3-(Tritylamino)phenyl]ethanolHCID 66770330—
SolventDichloromethaneHCID 6344—
Product4-Nitrobenzenesulfonic Acid 2-[3-(Tritylamino)phenyl]ethyl EsterHCID 86646960100%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 2-[3-(tritylamino)phenyl]ethanol (5.00 g, 13.2 mmol) and triethylenediamine (2.22 g, 19.8 mmol) in DCM (52.7 mL) under nitrogen at 0° C. was added portion-wise p-nitrobenzenesulfonyl chloride (3.50 g, 15.8 mmol) over a period of 5 min. The resulting mixture stirred at 0° C. for 40 min and then saturated aqueous sodium bicarbonate solution (˜50 mL) was added. The mixture was stirred at room temperature for 10 min and then the layers were separated. The aqueous layer was extracted with DCM (2ט50 mL) and the combined organic layers were dried over sodium sulfate, filtered, and concentrated under reduced pressure to give the title compound (7.44 g, 100% yield) as an orange-yellow foamy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816088B2
Source datasetuspto-grants-2014_08
ORD IDord-57512e5298b54796aaf7ce24fd64ef97
Source noteuspto-grants-2014_08