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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500474Generated: October 26, 2026

Tributylphosphine → HCID 21867689, compound

https://huagongshe.com/reaction/500474

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 numberUS07772229B2
Source datasetuspto-grants-2010_08
ORD IDord-7818e6525b6747d99031eec9cc1b8562
Source noteuspto-grants-2010_08