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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595918Generated: November 1, 2026

Triethylamine → [3-(2-Methanesulfonylamino-ethyl)-phenyl]-acetic acid tert-butyl ester

https://huagongshe.com/reaction/1595918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant[2-(2-Amino-ethyl)-phenyl]-acetic acid tert-butyl esterHCID 54411372—
SolventDichloromethaneHCID 6344—
Product[3-(2-Methanesulfonylamino-ethyl)-phenyl]-acetic acid tert-butyl esterHCID 5417023495.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of [2-(2-amino-ethyl)-phenyl]-acetic acid tert-butyl ester (422.5 mg, 1.795 mmol), triethylamine (908 mg, 8.977 mmol), and methanesulfonyl chloride (226.2 mg, 1.975 mmol) in CH2Cl2 (20 mL) was combined and stirred at 0° C. for 18 h. The organic solution was washed consecutively with dilute HCl, water, saturated NaHCO3, and brine. The organic solution was dried over MgSO4, filtered, and concentrated to provide the title sulfonamide (535 mg). MS 331 (M+18).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288120B1
Source datasetuspto-grants-2001_09
ORD IDord-5fc8523065fa472a85f0eb0f63eebd7a
Source noteuspto-grants-2001_09