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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15770Generated: October 25, 2026

Triethylamine → 3-Nitrophenethyl methanesulfonate

https://huagongshe.com/reaction/15770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-Nitrophenylethyl alcoholHCID 104058—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-Nitrophenethyl methanesulfonateHCID 2197388484%

Reaction Steps

Methanesulfonyl chloride (0.28 mL) was added dropwise to a stirred solution of 2-(3-nitrophenyl)ethanol (0.5 g; 1 eq) in dichloromethane (3 mL) and triethylamine (0.5 mL; 1.2 eq) at 0° C. under an inert atmosphere. The solution was allowed to reach r.t. and stirred for 5 hours. The reaction mixture was diluted with water (3 mL) and extracted into dichloromethane (3×3 mL). The organic layers were combined, dried over Na2SO4 and concentrated under reduced pressure. The crude was purified by flash chromatography, eluting with a gradient from dichloromethane to dichloromethane/MeOH (98/2) affording the title compound in 84% yield (0.62 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732600B2
Source datasetuspto-grants-2010_06
ORD IDord-b0d83144ac3a492fa8c9af88da90f448
Source noteuspto-grants-2010_06