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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820006Generated: October 27, 2026

Vanillin → 2-Phenoxyacetamide

https://huagongshe.com/reaction/1820006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVanillinHCID 1183—
ReactantPropionitrileHCID 7854—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-n-(4-bromophenyl)acetamideHCID 225526—
SolventEthyl AcetateHCID 8857—
Product2-PhenoxyacetamideHCID 69314190%

Reaction Conditions

Temperature80 °C

Reaction Steps

To 4-hydroxy-3-methoxybenzaldehyde (2.02 g, 13.3 mmol), 2-bromo-N-(4-bromophenyl)acetamide (3.00 g, 10.2 mmol) and potassium carbonate (2.12 g, 15.4 mmol) was added propionitrile (10 ml), and the mixture was stirred at 80° C. for one day. The reaction mixture was diluted with ethyl acetate, washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by alumina column chromatography (developing solvent; ethyl acetate), and powderized with ethyl acetate-diisopropyl ether (1:5) to give a phenoxyacetamide derivative (2.93 g). The title compound was obtained by similar operations as in Reference Example 43 and Example 6 and using this compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601868B2
Source datasetuspto-grants-2009_10
ORD IDord-a87d2fb6c4d143778be2bab68757a9a6
Source noteuspto-grants-2009_10