HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-2-nitrobenzene → O-(o-Aminophenoxy)benzoic acid lactam
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-2-nitrobenzene | HCID 6945 | — |
| Reactant | Potassium salicylaldehyde | HCID 86750311 | — |
| Product | O-(o-Aminophenoxy)benzoic acid lactam | HCID 72374 | — |
Reaction Steps
The starting material 10,11-dihydro-dibenz[b,f][1,4]oxazepin-11-one was prepared according to the procedures reported in Coyne et al (J. Med. Chem., 1967, 10:541). Briefly, this entailed coupling potassium salicylaldehyde with 2-chloronitrobenzene, followed by oxidation to the carboxylic acid, reduction of nitro, and finally ring closure, to yield the desired starting material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05834459 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-9519089090734e9f908f4bf9173e37f5 |
| Source note | uspto-grants-1998_11 |