HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261301Generated: October 27, 2026
2-Nitrotoluene → alpha-Bromo-2-nitrotoluene
https://huagongshe.com/reaction/261301
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%. Continuation of the bromination did not prove advantageous. The process described in German Democratic Republic patent specification No. 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 a benzal bromide or a complete bromination of o-nitrotoluene as starting material to benzyl bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04165268 |
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| Source dataset | uspto-grants-1979_08 |
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| ORD ID | ord-bfd0ff083e8040ba991d0803126b7b09 |
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| Source note | uspto-grants-1979_08 |
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