Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411527Generated: October 25, 2026

Tributylphosphine → HCID 21867689, compound

https://huagongshe.com/reaction/411527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant3,4-DimethoxyphenolHCID 16251—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant4-(1-Hydroxy-3-butenyl)benzonitrileHCID 11019345—
SolventTolueneHCID 1140—
ProductHCID 21867689HCID 2186768968.6%

Reaction Steps

A cooled (0° C.) mixture of 4-(1-hydroxy-3-butenyl)benzonitrile (14.6 g, 84.3 mmol) and 3,4-dimethoxyphenol (19.5 g, 125.4 mmol) in toluene (500 mL) was treated with tributylphosphine (32.14 mL of 97% purity, 25.6 g, 126.4 mmol), followed by 1,1′-(azodicarbonyl)dipiperidine (31.8 g, 126.4 mmol). After addition was complete, the reaction mixture thickened and the temperature rose to 15° C. Additional toluene was added (500 mL), and the mixture stirred at rt overnight. The precipitate of tributylphosphine oxide was then removed by filtration and the filtrate concentrated in vacuo to give 65.8 g of crude product. This was purified by chromatography on silica gel, eluting with toluene:methanol (98:2), to yield 17.9 g of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559162B2
Source datasetuspto-grants-2003_05
ORD IDord-ee1c3e3fccbc4cb3a9c716dc9a366598
Source noteuspto-grants-2003_05