Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479200Generated: October 30, 2026

Potassium Iodide → [Rac]-2-ethoxy-3-[4-(5-methyl-2-thiophen-2-yl-oxazol-4-ylmethoxy)-benzofuran-7-yl]-propionic acid methyl ester

https://huagongshe.com/reaction/479200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2-ThiophenecarboxaldehydeHCID 7364—
ReactantPotassium CarbonateHCID 11430—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant4-(Chloromethyl)-5-methyl-2-(thiophen-2-yl)-1,3-oxazoleHCID 5076491—
Reactant2-Ethoxy-3-(4-hydroxy-benzofuran-7-yl)-propionic acid methyl esterHCID 68617212—
Product[Rac]-2-ethoxy-3-[4-(5-methyl-2-thiophen-2-yl-oxazol-4-ylmethoxy)-benzofuran-7-yl]-propionic acid methyl esterHCID 69556807—

Reaction Steps

In analogy to the procedure described in example 120 f], 2-ethoxy-3-(4-hydroxy-benzofuran-7-yl)-propionic acid methyl ester (example 120 e]) was reacted with 4-chloromethyl-5-methyl-2-thiophen-2-yl-oxazole (prepared from thiophen-2-carbaldehyde and diacetyl monoxyme followed by treatment with POCl3 in analogy to the procedures described in examples 21 a] and b]) in the presence of potassium carbonate and potassium iodide to yield [rac]-2-ethoxy-3-[4-(5-methyl-2-thiophen-2-yl-oxazol-4-ylmethoxy)-benzofuran-7-yl]-propionic acid methyl ester, which was further saponified in analogy to the procedure described in example 120 f] to yield [rac]-2-ethoxy-3-[4-(5-methyl-2-thiophen-2-yl-oxazol-4-ylmethoxy)-benzofuran-7-yl]-propionic acid as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642389B2
Source datasetuspto-grants-2003_11
ORD IDord-dfefb11a730f4938b744bdcc7b9c3d82
Source noteuspto-grants-2003_11