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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 48551Erstellt: 24. Oktober 2026

Hydrochloric Acid → Perillaldehyde

https://huagongshe.com/de/reaction/48551

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2-NitrobenzaldehydeHCID 11101—
EduktAluminum isopropoxideHCID 11143—
EduktPerilla alcoholHCID 369312—
LösungsmittelBenzeneHCID 241—
LösungsmittelEthyl AcetateHCID 8857—
ProduktPerillaldehydeHCID 1644184%

Reaktionsschritte

(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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06703527B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-3b9cccf736d040ea8ba2282804b3798f
Quellennotizuspto-grants-2004_03