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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596710Generated: November 1, 2026

Tri-o-tolylphosphine → HCID 67580760, compound

https://huagongshe.com/reaction/1596710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTri-o-tolylphosphineHCID 80271—
Reactant2-ButenaMide, N,N-diethyl-, (E)-HCID 5354453—
ReactantHCID 21702602HCID 21702602—
Catalystpalladium(II) acetateHCID 167845—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 67580760HCID 67580760—

Reaction Steps

A solution of 2-[5-bromo-2-[2,6-difluorobenzyloxy)phenyl]-1-ethanol (14.07 g, 41.02 mmol) and N,N-diethylcrotonamide (8.68 g, 61.53 mmol) in 60 mL triethylamine in a thick-walled pyrex tube is degassed wish nitrogen for 15 minutes. Pd(OAc)2 (0.46 g, 2.05 mmol) and tri-o-tolylphosphine (1.25 g, 4.10 mmol) are placed into the tube, which is then sealed, and the mixture is heated to 100° for 5 hours. The mixture is diluted with EtOAc (400 mL), and white precipitate is filtered out. The filtrate is then washed with 1 N HCl (2×400 mL), H20 (1×100 mL) and brine (1×100 ni), dried over MgSO4, and concentrated in vacuo. Chromatography (silica, 3:1 EtOAc/hexane) gives (E)-3-[4-(2,6-difluorobenzyloxy)-3-(2-hydroxyethyl)-phenyl]-2-butenoic acid diethy amide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291530B1
Source datasetuspto-grants-2001_09
ORD IDord-c1f1db60bfaa434794c8e7f4afa8bfaa
Source noteuspto-grants-2001_09