Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514770Generated: October 30, 2026

Triethylamine → 2-{[(2-Nitrophenyl)sulfonyl]amino}ethyl methanesulfonate

https://huagongshe.com/reaction/514770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN-(2-hydroxyethyl)-2-nitrobenzenesulfonamideHCID 3102011—
ReactantEthyl acetate hexaneHCID 21226206—
SolventEthyl AcetateHCID 8857—
Product2-{[(2-Nitrophenyl)sulfonyl]amino}ethyl methanesulfonateHCID 86635903—

Reaction Conditions

Temperature10 °C

Reaction Steps

Triethylamine (20 mL, 144.6 mmol) was added to a solution of compound 54 (29.5 g, 119.9 mmol) in ethyl acetate (300 mL). The mixture was cooled to 10° C. in an ice bath. Then, a solution of mesyl chloride (10.2 mL, 131.8 mmol) in ethyl acetate (50 mL) was added dropwise at a temperature ≦20° C. The resulting solution was stirred at room temperature for 3 h (TLC monitoring, eluent: hexane-ethyl acetate, 4:1). The reaction mixture was filtered to remove the precipitate-triethylamine hydrochloride. The filtrate was washed with aqueous NaHCO3, water, and evaporated. Yield of 55: 32.2 g (83%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108916B2
Source datasetuspto-grants-2015_08
ORD IDord-612a917d996b4eb1b1be5063b1d96cbf
Source noteuspto-grants-2015_08