HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Nitrotoluene → alpha-Bromo-2-nitrotoluene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Nitrotoluene | HCID 6944 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Tetrachloromethane--water (1/1) | HCID 17768942 | — |
| Product | alpha-Bromo-2-nitrotoluene | HCID 77569 | 45% |
Reaction Steps
Even the side-chain brominations of o-nitrotoluene in a carbon tetrachloride/water mixture using elementary bromine and under UV-irradiation, which have been described recently in German Democratic Republic patent specifications Nos. 74279 and 82463, provide only o-nitrobenzyl bromide in a yield of 45 to 55%. The process described in German Democratic Republic patent specification 118609 affords a somewhat better yield when o-nitrotoluene is brominated in carbon tetrachloride under irradiation with visible or ultra-violet light or using peroxide as catalyst; but in this process too it was not possible to obtain either o-nitrobenzal bromide or a complete sidechain bromination of o-nitrotoluene to yield o-nitrobenzyl bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04191621 |
| Source dataset | uspto-grants-1980_03 |
| ORD ID | ord-fba3f5e2a4a74ffab95da40ab0e343e3 |
| Source note | uspto-grants-1980_03 |