Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699021Generated: October 31, 2026

Ethyl bromoacetate → [2-(2-Methanesulfonylamino-ethyl)-phenoxy]-acetic Acid Ethyl Ester

https://huagongshe.com/reaction/1699021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant2-NaphthylalanineHCID 185915—
ReactantN-[2-(2-hydroxy-phenyl)-ethyl]-methanesulfonamideHCID 22246821—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product[2-(2-Methanesulfonylamino-ethyl)-phenoxy]-acetic Acid Ethyl EsterHCID 5398738213.3%

Reaction Steps

A mixture of N-[2-(2-hydroxy-phenyl)-ethyl]-methanesulfonamide (4.3 g, 20 mmol), Nal (1.2 g, 8.0 mmol), K2CO3 (6.07 g, 44 mmol), ethyl bromoacetate (3.34 g, 20 mmol), and DMF (70 mL) was stirred at room temperature for 24 h. The reaction was poured into water and the aqueous solution was extracted with CH2Cl2. The organic solution was washed with water (1×) followed by brine (1×). The organic solution was dried (MgSO4), filtered, and concentrated. Flash chromatography (hexanes to 7:3 hexanes:EtOAc) provided the title compound (800 mg). 1H NMR (400 MHz, CDCl3) δ7.18 (m, 2H), 6.93 (t, 1H), 6.71 (d, 1H), 4.97 (m, 1H), 4.65 (s, 2H), 4.24 (q, 2H), 3.42 (m, 2H), 2.94 (t, 2H), 2.75 (s, 3H), 1.27 (t, 3H); MS 319 (M+18).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344485B1
Source datasetuspto-grants-2002_02
ORD IDord-86a1f4fcf65a4dbba694763929d91f57
Source noteuspto-grants-2002_02