HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminophenol → HCID 10904161, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminophenol | HCID 5801 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 9946252 | HCID 9946252 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10904161 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05961960 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-e23f46c42bcb4ac4be3300f036f5768f |
| Source note | uspto-grants-1999_10 |