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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100533Generated: October 29, 2026

Ethyl iodoacetate → [2-(2-Chloro-6-fluoro-phenyl)-ethoxy]-acetic acid ethyl ester

https://huagongshe.com/reaction/2100533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl iodoacetateHCID 12183—
Reactant2,6-Di-tert-butylpyridineHCID 68510—
Reactant2-(2-Chloro-6-fluorophenyl)ethanolHCID 2733235—
CatalystSilver(I) trifluoromethanesulfonateHCID 76223—
Product[2-(2-Chloro-6-fluoro-phenyl)-ethoxy]-acetic acid ethyl esterHCID 68564810—

Reaction Steps

In analogy to the procedure described in example 78.1, 2-(2-chloro-6-fluoro-phenyl)-ethanol was reacted with ethyl iodoacetate in the presence of silver trifluoromethanesulfonate and 2,6-di-tert-butylpyridin to give [2-(2-chloro-6-fluoro-phenyl)-ethoxy]-acetic acid ethyl ester as colorless liquid. 1H NMR (CDCl3): 1.28 (t, J=7.1 Hz, 3H), 3.15 (t, J=7.1 Hz, 2H), 3.73 (t, J=7.3 Hz, 2H), 4.11 (s, 2H), 4.22 (q, J=7.1 Hz, 2H), 6.96 (m, 1H), 7.09-7.19 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572801B2
Source datasetuspto-grants-2009_08
ORD IDord-52554209fc5a4679b5c26c45f7c589c9
Source noteuspto-grants-2009_08