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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390735Generated: October 29, 2026

Methanol → Phenol, 2-[[(2-hydroxyphenyl)imino]methyl]-

https://huagongshe.com/reaction/390735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-AminophenolHCID 5801—
Reactant2-Hydroxy-1-naphthaldehydeHCID 12819—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductPhenol, 2-[[(2-hydroxyphenyl)imino]methyl]-HCID 74479—

Reaction Steps

The preparations of compounds used in this invention are shown in detail below. In general [nBu4N][OsVI(N)Cl4] is reacted with the ligand in a suitable organic solvent, such as methanol, ethanol or dichloromethane. The Schiff base ligands 5-X—H2salpa (salpa=N-salicylidene-2-aminophenol dianions) are synthesized by condensation of the appropriate 2-hydroxybenzyaldehyde with the 2-aminophenol in refluxing ethanol. The Schiff base ligand nalph is synthesized by condensation of the 2-hydroxy-1-naphthaldehyde with the 2-aminophenol in refluxing ethanol. [NnBu4][OsVI(N)Cl4] were prepared by a literature procedure (Griffith, W. P. and Pawson, D. J. J. Chem. Soc., Dalton Trans. 1973, 1315.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383673B2
Source datasetuspto-grants-2013_02
ORD IDord-b9b91f71ceec4cf09f066b0829d25792
Source noteuspto-grants-2013_02