Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168614Generated: October 26, 2026

4-Benzyloxy-N-methoxy-N-methylphenylacetamide → 1-(4-Benzyloxy-phenyl)-pentan-2-one

https://huagongshe.com/reaction/2168614

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyloxy-N-methoxy-N-methylphenylacetamideHCID 11254648—
ReactantHCID 178455851HCID 178455851—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Benzyloxy-phenyl)-pentan-2-oneHCID 67373361—

Reaction Steps

To a stirred solution of 2-(4-benzyloxy-phenyl)-N-methoxy-N-methyl-acetamide (10.51 mmol, 3.0 g) in anhydrous THF at 0° C. was added n-propyl magnesium bromide (2.0 M solution in THF, 20 mL) drop-wise over 30 min. After completion of addition, the reaction mixture was warmed to room temperature and stirred for 30 min. The reaction mixture was cooled to 0° C. and quenched by adding saturated aqueous NH4Cl drop-wise followed by addition of ethyl acetate. The organic layer was separated, dried, filtered, and concentrated under reduced pressure. The residue was purified by flash column chromatography by eluting with 5% ethyl acetate in hexanes to provide 1-(4-benzyloxy-phenyl)-pentan-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045461B2
Source datasetuspto-grants-2015_06
ORD IDord-8773dda47d8d409f8c19d9fb9c28da01
Source noteuspto-grants-2015_06