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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261301Generated: October 27, 2026

2-Nitrotoluene → alpha-Bromo-2-nitrotoluene

https://huagongshe.com/reaction/261301

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitrotolueneHCID 6944—
ReactantBromineHCID 24408—
ReactantTetrachloromethane--water (1/1)HCID 17768942—
Productalpha-Bromo-2-nitrotolueneHCID 7756945%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04165268
Source datasetuspto-grants-1979_08
ORD IDord-bfd0ff083e8040ba991d0803126b7b09
Source noteuspto-grants-1979_08