HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → HCID 178433883, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | HCID 178433880 | HCID 178433880 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178433883 | HCID 178433883 | 96% |
Reaction Steps
3′-[(2Z)-[1-(3,4-dimethylphenyl)-1,5-dihydro-3-methyl-5-oxo-4H-pyrazol-4-ylidene]hydrazino]-2′-hydroxy-[1,1′-biphenyl]-3-carboxylic acid, 8 g of crude orange solid, was suspended at room temperature in ethanol (800 ml) under a nitrogen atmosphere. Ethanolamine (2.2 ml, −2 molar equivalents) was added via syringe over 5 minutes. The resulting dark red suspension was stirred at room temperature for 45 hours and the solid isolated by filtration, washed with ethanol (10 ml×2) and dried at 50° C. in a vacuum oven over night to yield 9.83 g (96% yield) of the title compound. NMR similar to Example 1; ethanol content 1.3% w/w but no THF present.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846024B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-8d1f628489ca4f0bb565c5d0563b2b7d |
| Source note | uspto-grants-2014_09 |