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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367074Generated: October 30, 2026

Triphenylphosphine → alpha-Methylcinnamic alcohol

https://huagongshe.com/reaction/2367074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
Reactant3-Phenyl-2-methylacroleinHCID 5354896—
ReactantHCID 178418361HCID 178418361—
Productalpha-Methylcinnamic alcoholHCID 639384694%

Reaction Steps

Into a stainless steel autoclave equipped with a glass inner tube, Cu(NO3)(PPh3)2 (11.7 mg, 0.018 mmol) and triphenylphosphine (28.3 mg, 0.108 mmol) were introduced. The inside of the autoclave was then replaced with nitrogen. To the autoclave, an ethanolic solution of sodium hydroxide (0.03 M) (6.0 mL, 0.18 mmol) and α-methyl cinnamic aldehyde (1.26 mL, 9 mmol) were added, and stirring was performed at a hydrogen pressure of 5 MPa at 50° C. for 16 hours. The hydrogen was released with great care, and the conversion was analyzed by GC (>99%). The contents were concentrated, and then purified by silica gel chromatography. Thus, 1.25 g of the α-methyl cinnamic alcohol was obtained (yield: 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697881B2
Source datasetuspto-grants-2014_04
ORD IDord-3082572c50a94bb6a7db673e916b7932
Source noteuspto-grants-2014_04