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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168588Generated: October 30, 2026

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

https://huagongshe.com/reaction/2168588

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyloxy-N-methoxy-N-methylphenylacetamideHCID 11254648—
ReactantHCID 178418265HCID 178418265—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Benzyloxy-phenyl)-hexan-2-oneHCID 67373414—

Reaction Steps

To a stirred solution of 2-(4-benzyloxy-phenyl)-N-methoxy-N-methyl-acetamide (42.1 mmol, 12.0 g) in anhydrous THF at −10° C. was added n-butyl magnesium chloride (2.0 M solution in THF, 92.6 mmol, 46.3 mL) drop-wise. 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 with 1.0 N HCl by adding drop-wise. The reaction mixture was poured into water, extracted with ethyl acetate, and the combined extract was washed with water followed by brine. The organic layer was dried (Na2SO4), filtered and concentrated under reduced pressure. The resultant residue was purified by column chromatography using 10% ethyl acetate in hexanes to provide 1-(4-benzyloxy-phenyl)-hexan-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045461B2
Source datasetuspto-grants-2015_06
ORD IDord-92a04b9cbcc84fa9a39f178d86c7e57c
Source noteuspto-grants-2015_06