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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330329Generated: November 1, 2026

Pyridine → HCID 19869783, compound

https://huagongshe.com/reaction/330329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantHCID 19869782HCID 19869782—
SolventDichloromethaneHCID 6344—
ProductHCID 19869783HCID 1986978394.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 14.4 grams (0.065 mole) of 3,4-difluoromethylenedioxybenzoyl chloride in 150 mL of methylene chloride was stirred and cooled to 0° C. To this was added 6.4 grams (0.066 mole) of O,N-dimethylhydroxylamine hydrochloride, followed by the dropwise addition of 11.0 mL (0.136 mole) of pyridine. Upon completion of addition the reaction mixture was stirred at ambient temperature for 18 hours. The reaction mixture was washed with two portions of aqueous 10% hydrochloric acid, two portions of aqueous IN sodium hydroxide, and two portions of an aqueous saturated solution of sodium chloride. The organic layer was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to yield 15.1 grams of N-methyl-N-methoxy-3,4-difluoromethylenedioxybenzamide. The nmr spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04895871
Source datasetuspto-grants-1990_01
ORD IDord-1038ac0034da4f6cba31ee659c7a6ae8
Source noteuspto-grants-1990_01