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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1007621Erstellt: 23. Oktober 2026

Pivalic anhydride → 3-(3-Hydroxy-4-methoxyphenyl)prop-2-enal

https://huagongshe.com/de/reaction/1007621

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPivalic anhydrideHCID 15234—
Edukt3-(3-Hydroxy-4-methoxyphenyl)prop-2-enoic acidHCID 92126—
EduktHCID 178418361HCID 178418361—
KatalysatorPhosphine, tris(4-methylphenyl)-HCID 13956—
Katalysatorpalladium(II) acetateHCID 167845—
Produkt3-(3-Hydroxy-4-methoxyphenyl)prop-2-enalHCID 5402515749,4%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Palladium acetate (58 mg, 0.257 mmol), tri(p-tolyl) phosphine (157 mg, 0.515 mmol), 3-hydroxy-4-methoxycinnamic acid (5.00 g, 25.7 mmol) and pivalic acid anhydride (14.4 g, 77.2 mmol) were added thereto, and thereafter the mixture was bubbled with nitrogen gas for 30 minutes to substitute nitrogen gas completely for the gas in the system of reaction, whereby the system was filled with nitrogen gas. Next, hydrogen gas was added thereinto to substitute hydrogen gas for the gas in the system, and then the mixture was stirred under hydrogen pressure of 3.4 MPa at 80° C. for 24 hours for reaction. Thus obtained reaction solution was concentrated under reduced pressure to remove tetrahydrofuran by vaporization. The remaining residue was subjected to a purification process with a silica gel column chromatography (eluting solvent: toluene/ethyl acetate=4/1) to obtain 3-hydroxy-4-methoxycinnamaldehyde (2.26 g, 12.7 mmol, yield: 49%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06794531B2
Quelldatensatzuspto-grants-2004_09
ORD IDord-5fbb8291ec95476a9ec895955de679cc
Quellennotizuspto-grants-2004_09