HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 5-Chloro-6-nitro-2-phenyl-1,3-benzoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Methane | HCID 297 | — |
| Reactant | 2-Amino-4-chloro-5-nitrophenol | HCID 3894848 | — |
| Product | 5-Chloro-6-nitro-2-phenyl-1,3-benzoxazole | HCID 13609246 | — |
Reaction Steps
To a flask equipped with a vigreux column was added 2-amino-4-chloro-5-nitro-phenol, benzaldehyde, Darco KB and xylenes. The mixture was then refluxed overnight and the mixture was cooled, filtered and the solvent removed under vacuum. The resultant solid was recrystallized from Et2O to yield 5-chloro-6-nitro-2-phenyl-benzooxazole which was subjected to the procedure from Example 349B substituting 5-chloro-6-nitro-2-phenyl-benzooxazole for the product from Example 349A to provide the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07910595B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-4eeaa7693a61453aa658627e4146e84c |
| Source note | uspto-grants-2011_03 |