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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100484Generated: October 30, 2026

Ethyl iodoacetate → HCID 68568603, compound

https://huagongshe.com/reaction/2100484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl iodoacetateHCID 12183—
Reactant2,6-Di-tert-butylpyridineHCID 68510—
Reactant4-Fluorophenethyl AlcoholHCID 82068—
CatalystSilver(I) trifluoromethanesulfonateHCID 76223—
ProductHCID 68568603HCID 68568603—

Reaction Steps

In analogy to the procedure described in example 78.1, 2-(4-fluoro-phenyl)-ethanol was reacted with ethyl iodoacetate in the presence of silver trifluoromethanesulfonate and 2,6-di-tert-butylpyridin to give [2-(4-fluoro-phenyl)-ethoxy]-acetic acid ethyl ester as colorless liquid. 1H NMR (CDCl3): 1.28 (t, J=7.2 Hz, 3H), 2.92 (t, J=7.0 Hz, 2H), 3.73 (t, J=7.0 Hz, 2H), 4.07 (s, 2H), 4.22 (q, J=7.2 Hz, 2H), 6.97 (m, 2H), 7.21 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572801B2
Source datasetuspto-grants-2009_08
ORD IDord-2b475dde709f4f7297cf9a121ba4b998
Source noteuspto-grants-2009_08