HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2,3-Trichlorobenzene → 2,3-Dichloro-6-nitrobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2,3-Trichlorobenzene | HCID 6895 | — |
| Reactant | 2,3,4-Trichloronitrobenzene | HCID 28697 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Reactant | HCID 178508181 | HCID 178508181 | — |
| Product | 2,3-Dichloro-6-nitrobenzonitrile | HCID 2736020 | — |
Reaction Steps
As shown below in the Examples, a preferred process is set forth for making 2-amino-5,6-dichloro-3,4-dihydroquinazoline from commercially available starting materials. In one process 1,2,3-trichlorobenzene is used as the starting material and is nitrated using, for example, nitric/sulfuric acids to form 1,2,3-trichloro-4-nitrobenzene. This compound is then reacted with a cyanating agent such as CuCN to form 2,3-dichloro-6-nitrobenzonitrile. The nitrile is then reacted under reducing conditions using for example B2H6 to form 2,3-dichloro-6-nitrobenzylamine HCl which is then reduced and reacted with CNX to form the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06194420B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-ef58309f84144dda8660277dd5c84248 |
| Source note | uspto-grants-2001_02 |