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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367075Generated: October 30, 2026

Triphenylphosphine → alpha-Methylcinnamic alcohol

https://huagongshe.com/reaction/2367075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
Reactant3-Phenyl-2-methylacroleinHCID 5354896—
ReactantHCID 178418361HCID 178418361—
SolventIsopropanolHCID 3776—
Productalpha-Methylcinnamic alcoholHCID 639384685%

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 isopropyl alcohol solution of sodium hydroxide (0.03 M) (6.0 mL, 0.18 mmol), and α-methyl cinnamic aldehyde (0.50 mL, 3.6 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, 453 mg of the α-methyl cinnamic alcohol was obtained (yield: 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697881B2
Source datasetuspto-grants-2014_04
ORD IDord-5823b75b64244b4e996acd63957cbe9c
Source noteuspto-grants-2014_04