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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108879Generated: October 31, 2026

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

https://huagongshe.com/reaction/1108879

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Phenylprop-2-En-1-OlHCID 308—
ReactantVeratraldehydeHCID 8419—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant6-benzothiazolesulfonic acid, 2,2'-azinobis(3-ethyl-2,3-dihydro-, diammonium saltHCID 9570474—
SolventEthanolHCID 702—
Product3-Phenylprop-2-EnalHCID 30748%

Reaction Steps

213 mg (1.59 mmol) of 3-phenyl-2-propen-1-ol in 1.1 ml of ethanol were treated at 45° C. with stirring into 22 ml of buffer solution (see Example 1) with 24.3 mg (0.180 mmol) of 1-hydroxy-1H-benzotriazole. After approx. 10 minutes, 5 ml of an aqueous solution of 2 mg/ml laccase from Trametes versicolor (specific activity approx. 18 IU/mg, defined with ABTS as the substrate) were added. After 3 hours in contact with the air, 48% of 3-phenyl-2-propenal were formed (GC analysis), and a further 24.3 mg of HOBT and 5 ml of laccase solution were added. GC analysis after 6 hours revealed complete conversion into 3-phenyl-2-propenal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069282
Source datasetuspto-grants-2000_05
ORD IDord-f9420b491535469293570265e0ab7cd1
Source noteuspto-grants-2000_05