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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48551Generated: October 26, 2026

Hydrochloric Acid → Perillaldehyde

https://huagongshe.com/reaction/48551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-NitrobenzaldehydeHCID 11101—
ReactantAluminum isopropoxideHCID 11143—
ReactantPerilla alcoholHCID 369312—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
ProductPerillaldehydeHCID 1644184%

Reaction Steps

(S)-(−)-Perillyl alcohol (300 mg, 2.0 mmol) was dissolved in benzene (1 mL), added with aluminum isopropoxide (40 mg, 0.1 eq, 0.20 mmol) and 2-nitrobenzaldehyde (390 mg, 1.3 eq, 2.6 mmol) and stirred at room temperature for 2 hours. The reaction mixture was added with ethyl acetate and made acidic with addition of 2 N hydrochloric acid, and then the organic layer was separated. Subsequently, the organic layer was washed with saturated brine and dried over magnesium sulfate. The solvent was evaporated in vacuo, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=30:1) to obtain 250 mg (yield: 84%) of the title compound as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06703527B2
Source datasetuspto-grants-2004_03
ORD IDord-3b9cccf736d040ea8ba2282804b3798f
Source noteuspto-grants-2004_03