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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298158Generated: October 30, 2026

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

https://huagongshe.com/reaction/2298158

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) δ 7.18 (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 numberUS06492412B2
Source datasetuspto-grants-2002_12
ORD IDord-ab3761190d4d4d929b449b363e90f941
Source noteuspto-grants-2002_12