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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394302Generated: October 29, 2026

Triphenylphosphine → HCID 68617614, compound

https://huagongshe.com/reaction/394302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 20110334HCID 20110334—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 22647515HCID 22647515—
Reactant[Rac]-2-ethoxy-3-(3-fluoro-4-hydroxy-phenyl)-propionic acid ethyl esterHCID 68618019—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68617614HCID 68617614—

Reaction Steps

In analogy to the procedure described in example 1 d], [rac]-2-ethoxy-3-(3-fluoro-4-hydroxy-phenyl)-propionic acid ethyl ester (example 7 a]) was reacted with 2-(2-p-tolyl-thiazol-4-yl)-ethanol (prepared from (2-p-tolyl-thiazol-4-yl)-acetic acid ethyl ester [Collection of Czechoslovak Chemical Communications (2001), 66(12), 1809-1830] with lithium aluminium hydride in analogy to the procedure described in example 12 b]) in tetrahydrofuran in the presence of triphenylphosphine and DEAD (diethyl azodicarboxylate) to yield [rac]-2-ethoxy-3-{3-fluoro-4-[2-(2-p-tolyl-thiazol-4-yl)-ethoxy]-phenyl}-propionic acid ethyl ester, which was further saponified in analogy to the procedure described in example 4 e], to yield [rac]-2-ethoxy-{3-fluoro-4-[2-(2-p-tolyl-thiazol-4-yl)-ethoxy)-phenyl}-propionic acid as light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809110B2
Source datasetuspto-grants-2004_10
ORD IDord-397dd8414f1046a6a05b91b342101ec9
Source noteuspto-grants-2004_10