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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367077Generated: October 31, 2026

2-Phenylpropanal → 2-Phenyl-1-propanol

https://huagongshe.com/reaction/2367077

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PhenylpropanalHCID 7146—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178418361HCID 178418361—
Product2-Phenyl-1-propanolHCID 1429558.3%

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 2-phenylpropionaldehyde (1.21 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 (95%). The contents were concentrated, and then purified by silica gel chromatography. Thus, 715 mg of 2-phenyl-1-propanol was obtained (yield: 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697881B2
Source datasetuspto-grants-2014_04
ORD IDord-35a4b94d19ec494a913a286a0e1d94ff
Source noteuspto-grants-2014_04