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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356467Generated: October 26, 2026

Pyridine → 3-(4-Benzyloxy-phenyl)-N-methoxy-N-methyl-propionamide

https://huagongshe.com/reaction/356467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant3-(4-Benzyloxyphenyl)propionic acidHCID 561372—
SolventThionyl ChlorideHCID 24386—
Product3-(4-Benzyloxy-phenyl)-N-methoxy-N-methyl-propionamideHCID 18798659—

Reaction Steps

3-(4-Benzyloxyphenyl) propionic acid prepared in Example S (30 g, 117 mmol) was taken up in 300 mL of thionyl chloride. The reaction was kept under reflux for 5 hours, then cooled and concentrated. The residue was dissolved in 300 mL of CH2Cl2 and treated with N,O-dimethylhydroxylamine hydrochloride (14.1 g, 146 mmol) and 60 mL of pyridine at 0° C. The reaction was stirred overnight. The reaction was quenched with dilute HCl and extracted into EtOAc, and the organic layer was washed with sodium bicarbonate solution and dilute HCl and dried. The organic layer was dried (MgSO4) and concentrated. The residue was used further as crude reaction mixture or purified by flash silica gel column chromatography, eluting with EtOAc:hexane (1:9, then switching to 2:3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834506
Source datasetuspto-grants-1998_11
ORD IDord-2cedc33d0ff74e33835ad9a21efa296a
Source noteuspto-grants-1998_11