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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590113Generated: October 25, 2026

3-Benzyloxypyridine → N-amino-3-benzyloxypyridinium mesitylenesulfonate

https://huagongshe.com/reaction/1590113

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BenzyloxypyridineHCID 10012635—
ReactantO-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 11830845—
SolventDichloromethaneHCID 6344—
ProductN-amino-3-benzyloxypyridinium mesitylenesulfonateHCID 15257892—

Reaction Steps

A solution of O-mesitylenesulfonylhydroxylamine (13.7 g, 44.6 mmole, purity of 70%) in methylene chloride (150 ml) was added dropwise to a solution of 3-benzyloxypyridine (8.25 g, 44.6 mmole) in methylene chloride (150 ml) under ice-cooling, with stirring. The reaction solution was returned to room temperature, stirred for 1 hours and concentrated to one-quarter of the original volume at 20° to 30° C., and ether was added to the concentrate, thereby white crystals were precipitated. This product was used in the next reaction, without being purified.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05202334
Source datasetuspto-grants-1993_04
ORD IDord-a37ccfad46eb4f3ca7b8a6def85f67d4
Source noteuspto-grants-1993_04