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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743333Generated: October 28, 2026

Triphenylphosphine → HCID 19423911, compound

https://huagongshe.com/reaction/743333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-(Dimethylamino)-1-propanolHCID 76646—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 572468HCID 572468—
SolventDichloromethaneHCID 6344—
ProductHCID 19423911HCID 1942391136%

Reaction Steps

134 mg of 3-(N,N-dimethylamino)propanol and 342 mg of triphenyl phosphine were added to a solution of 230 mg of 2-(3-phenylpropyl)phenol (prepared as described in Preparation 29) in 10 ml of methylene chloride, and the mixture was cooled with ice and stirred. 227 mg of diethyl azodicarboxylate were then added dropwise to the solution, and the mixture was stirred at room temperature for 5 hours. At the end of this time, the solvent was removed by distillation under reduced pressure, and ethyl acetate and water were added to the residue and shaken. The ethyl acetate layer was separated and dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through silica gel, using a 10:1 by volume mixture of methylene chloride and methanol as the eluent, to give 115 mg (yield 36%) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556864
Source datasetuspto-grants-1996_09
ORD IDord-0947e3ec2eea4ecdacb9bac1969f3a13
Source noteuspto-grants-1996_09