Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737140Generated: October 31, 2026

2-Aminophenol → HCID 10904161, compound

https://huagongshe.com/reaction/1737140

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminophenolHCID 5801—
ReactantTriethylamineHCID 8471—
ReactantHCID 9946252HCID 9946252—
SolventEthanolHCID 702—
ProductHCID 10904161HCID 10904161—

Reaction Steps

28.2 g (0.12 mol) of 1-(2-ethylhexyl)-2-trichloromethylbenzimidazole (prepared by reacting N-2-ethylhexyl-o-phenylenediamine with trichloroacetamido methyl ester), 13.1 g (0.12 mot) of o-aminophenol and 39.4 g (0.38 mot) of triethylamine in 150 ml of ethanol are stirred at room temperature for 15 hours. The ethanol is subsequently removed on a rotary evaporator, ethyl acetate is added to the residue which remains, and the mixture is washed with water and dried over sodium sulfate. 35% of product is identified by BPLC in the product mixture thus ob-5 tained; isolation can be carried out, for example, by column chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05961960
Source datasetuspto-grants-1999_10
ORD IDord-e23f46c42bcb4ac4be3300f036f5768f
Source noteuspto-grants-1999_10