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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072709Generated: November 1, 2026

Triphenylphosphine → Ethyl (2R)-2-[4-(1-dodecyl-5-methyl-1H-pyrrol-2-yl)phenoxy]-3-phenylpropanoate

https://huagongshe.com/reaction/1072709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantEthyl phenyllactate, (-)-HCID 9877619—
Reactant4-(1-dodecyl-5-methyl-1H-pyrrol-2-yl)phenolHCID 22387704—
SolventTolueneHCID 1140—
ProductEthyl (2R)-2-[4-(1-dodecyl-5-methyl-1H-pyrrol-2-yl)phenoxy]-3-phenylpropanoateHCID 8658889233%

Reaction Steps

To a solution of 4-(1-dodecyl-5-methyl-1H-pyrrol-2-yl)phenol (2.97 g, 8.70 mmol), ethyl (S)-2-hydroxy-3-phenylpropanoate (1.86 g, 9.58 mmol) and triphenylphosphine (2.51 g, 9.57 mmol) in toluene (120 ml) was added diethyl azodicarboxylate (1.67 g, 9.57 mmol) and the mixture was refluxed for 20 hours under heating. The insoluble matter was filtered out and the filtrate was diluted with ethyl acetate. The obtained solution was washed with water and dried over magnesium sulfate anhydride, and the solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=8:1) to give the object compound as an oily substance. 1.49 g (yield: 33%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911468B2
Source datasetuspto-grants-2005_06
ORD IDord-f0d5fc47f90543568b514435fc4df75c
Source noteuspto-grants-2005_06