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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239543Generated: November 2, 2026

2-Methoxyethylamine → N-(2-methoxyethyl)-1-phenylmethanesulfonamide

https://huagongshe.com/reaction/2239543

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethylamineHCID 8018—
ReactantPhenylmethanesulfonyl chlorideHCID 74740—
SolventTetrahydrofuranHCID 8028—
ProductN-(2-methoxyethyl)-1-phenylmethanesulfonamideHCID 446732999.4%

Reaction Steps

Phenylmethanesulfonyl chloride (3.0 g, 15.7 mmol) was dissolved in dry THF (15 mL) and it was added dropwise to a solution of 2-methoxyethylamine (2.36 g, 31.5 mmol) in dry THF (50 mL) at 0° C. After addition the ice-bath was removed and the reaction was stirred at rt for 2.5 h. The solvent was removed in vacuo and the residue was dissolved in DCM. The mixture was washed with one portion of 5% aqueous HCl, several portions of water, dried through a phase separator and evaporated to give the title compound (3.58 g, 94%); 1H NMR (400 MHz, CDCl3): δ 7.43-7.35 (m, 5H), 4.52 (br s, 1H), 4.26 (s, 2H), 3.40 (t, 2H), 3.32 (s, 3H), 3.14-3.09 (m, 2H); Mass Spectrum: M−H+ 228.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723333B2
Source datasetuspto-grants-2010_05
ORD IDord-60be09b87bf34ee68b8021ef90f6750c
Source noteuspto-grants-2010_05