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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757502Generated: October 26, 2026

Pyridine → N,3,4,5-tetramethoxy-N-methyl-Benzamide

https://huagongshe.com/reaction/1757502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chloride, 3,4,5-trimethoxy-HCID 78282—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
SolventEthanolHCID 702—
ProductN,3,4,5-tetramethoxy-N-methyl-BenzamideHCID 26753597.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dissolve 3,4,5-trimethoxybenzoyl chloride (2.3 g, 10 mmol) and N,O-dimethylhydroxylamine hydrochloride (1.10 g, 11 mmol) in ethanol-free chloroform at room temperature. Cool the solution to 0° C. and add pyridine (1.85 g, 22 mmol). Stir at ambient temperature for 1 hour and evaporate the solvent in vacuo. Partition the residue between aqueous sodium chloride and a 1:1 mixture of ethyl ether and methylene chloride. Separate the organic phase, dry (Na2SO4), and evaporate the solvent in vacuo to yield an oil. Filter the oil through silica gel eluting with 65% ethyl acetate/hexane to yield 2.5 g of N-methoxy-N-methyl-(3,4,5-trimethoxy)benzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446068
Source datasetuspto-grants-1995_08
ORD IDord-b069b36463db499283f63e20862fef94
Source noteuspto-grants-1995_08