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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007621Generated: October 25, 2026

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

https://huagongshe.com/reaction/1007621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivalic anhydrideHCID 15234—
Reactant3-(3-Hydroxy-4-methoxyphenyl)prop-2-enoic acidHCID 92126—
ReactantHCID 178418361HCID 178418361—
CatalystPhosphine, tris(4-methylphenyl)-HCID 13956—
Catalystpalladium(II) acetateHCID 167845—
Product3-(3-Hydroxy-4-methoxyphenyl)prop-2-enalHCID 5402515749.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794531B2
Source datasetuspto-grants-2004_09
ORD IDord-5fbb8291ec95476a9ec895955de679cc
Source noteuspto-grants-2004_09