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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394731Generated: November 3, 2026

Potassium Iodide → (S)-3-{2-chloro-4-[2-(2-fluoro-phenyl)-5-methyl-oxazol-4-ylmethoxy]-phenyl}-2-ethoxy-propionic acid methyl ester

https://huagongshe.com/reaction/1394731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCesium carbonateHCID 10796—
ReactantPhosphorus oxychlorideHCID 24813—
Reactanto-FluorobenzaldehydeHCID 67970—
Reactant4-Chloromethyl-2-(2-fluoro-phenyl)-5-methyl-oxazoleHCID 4441114—
Reactant(2S)-3-(2-chloro-4-hydroxy-phenyl)-2-ethoxy-propionic acid methyl esterHCID 68616433—
Product(S)-3-{2-chloro-4-[2-(2-fluoro-phenyl)-5-methyl-oxazol-4-ylmethoxy]-phenyl}-2-ethoxy-propionic acid methyl esterHCID 69279900—

Reaction Steps

In analogy to the procedure described in example 1 f], (2S)-3-(2-chloro-4-hydroxy-phenyl)-2-ethoxy-propionic acid methyl ester (example 15 d]) was reacted with 4-chloromethyl-2-(2-fluoro-phenyl)-5-methyl-oxazole (prepared from 2-fluoro-benzaldehyde and diacetyl monoxyme followed by treatment with POCl3 in analogy to the procedures described in examples 5 a] and 2 b]) in the presence of cesium carbonate and potassium iodide to yield (S)-3-{2-chloro-4-[2-(2-fluoro-phenyl)-5-methyl-oxazol-4-ylmethoxy]-phenyl}-2-ethoxy-propionic acid methyl ester as colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348349B2
Source datasetuspto-grants-2008_03
ORD IDord-449dafc35a6042f1a8672f20df31f524
Source noteuspto-grants-2008_03