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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428706Generated: October 31, 2026

Methanesulfonyl chloride → 4-Nitrobenzyl methanesulfonate

https://huagongshe.com/reaction/1428706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-Nitrobenzyl alcoholHCID 69275—
SolventTolueneHCID 1140—
Product4-Nitrobenzyl methanesulfonateHCID 1892479472.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of (4-nitrophenyl)methanol (2 g, 13.06 mmol) in toluene (10 mL) was slowly added methane sulfonylchloride (1.21 mL, 15.67 mmol) at room temperature. The reaction mixture was heated to 80° C. for 4 h. TLC showed complete consumption of starting material. The reaction mixture was cooled to room temperature. The mixture was extracted with ethyl acetate and washed with water and brine. The extract was dried over magnesium sulfate and concentrated under reduced pressure. The crude was purified by column chromatography to give 4-nitrobenzyl methanesulfonate (2.2 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-7c882cb5e8844d5eae5059e6db5d9022
Source noteuspto-grants-2015_01