HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-5-nitrobenzene-1,3-dicarbonitrile → HCID 21559844, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-5-nitrobenzene-1,3-dicarbonitrile | HCID 13691769 | — |
| Reactant | HCID 21559842 | HCID 21559842 | — |
| Reactant | HCID 21559846 | HCID 21559846 | — |
| Reactant | Sodium hydroxide methanol | HCID 23721981 | — |
| Product | HCID 21559844 | HCID 21559844 | — |
Reaction Steps
2,6-Dicyano-4-nitro-phenol, used in Example 12, was prepared according to generally known processes: 2,6-dicyano-4-nitro-aniline is converted by a Sandmeyer reaction into 2,6-dicyano-4-nitro-chlorobenzene of melting point 218°-219.5°C, reacted with methanol/sodium hydroxide to give 2,6-dicyano-4-nitro-anisole of melting point 144°-148°C, and the latter subsequently split with sodium iodide in dimethylformamide to give 2,6-dicyano-4-nitro-phenol of melting point 228°-231°C. The last two stages correspond to a process indicated in Belgian Pat. No. 764,117.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03936447 |
| Source dataset | uspto-grants-1976_02 |
| ORD ID | ord-ae6d87d2c3f04b989dbbce6b76475ce2 |
| Source note | uspto-grants-1976_02 |