Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Amino-4-Nitrophenol | HCID 3613389 | — |
| Product | HCID 4137682 | HCID 4137682 | — |
Reaction Steps
To 11.5 grams (0.05 mole) of 3-nitrophenylchloroxime are added 150 milliliters of ethanol. To the mixture are added 23.1 grams (0.15 moles) of 2-amino-4-nitrophenol. The mixture is stirred under nitrogen at about 30° C. overnight and filtered to yield 2-(m-nitrophenyl)-5-nitrobenzoxazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06222044B1 |
|---|
| Source dataset | uspto-grants-2001_04 |
|---|
| ORD ID | ord-6bcc65375dca4547aa9a0e22bc3c1921 |
|---|
| Source note | uspto-grants-2001_04 |
|---|
