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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779284Generated: November 1, 2026

3-Phenylprop-2-En-1-Ol → Benzenepropanol

https://huagongshe.com/reaction/1779284

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Phenylprop-2-En-1-OlHCID 308—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
CatalystNickelHCID 935—
ProductBenzenepropanolHCID 31234—
ProductSodium BenzoateHCID 517055—
ProductHCID 19205590HCID 19205590—

Reaction Steps

Into a 300 ml nickel autoclave are charged cinnamyl alcohol (50.0 g, 0.37 mo1), sodium hydroxide (34.6 g, 0.43 mol), the catalyst of Example 2 (12.8 g catalyst suspended in 48.6 g water) and water (75 g). The autoclave is sealed and purged with nitrogen. The autoclave is heated under pressure of 1.0×106Pascals to 170° C. After hydrogen evolution ceases, the reaction product filtered and the basic filtrate is extracted with diethylether. The aqueous phase is acidified and extracted with ether. The acid and base extracts are evaporated and analyzed. The reaction yields sodium 3-phenylpropionate (69 mol percent), 3-phenylpropanol (25 mol percent) and sodium benzoate (8 mol percent).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05627125
Source datasetuspto-grants-1997_05
ORD IDord-031403b8500a44c389860f15a67db092
Source noteuspto-grants-1997_05