HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234763Generated: October 29, 2026
Hydrogen Bromide → 5-Bromo-2-methylbenzonitrile
https://huagongshe.com/reaction/234763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 5-Amino-2-methylbenzonitrile | HCID 2735365 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Bromo-2-methylbenzonitrile | HCID 12994004 | 44.5% |
Reaction Steps
15.2 g (0.22 mol) of sodium nitrite are heated to 70° C. in 160 ml of concentrated sulphuric acid and the solution formed is added dropwise to a solution of 26.4 g (0.2 mol) of the compound from Example XV in 400 ml of glacial acetic acid at 20° C. to 40° C. A solution of 63.1 g (0.44 mol) of copper(I) bromide in 400 ml of concentrated hydrobromic acid is added dropwise to this solution at 10° C. to 20° C. and the mixture is stirred for 0.5 hour. The reaction mixture is introduced into 11 of water, the precipitate which has separated out is filtered off with suction, washed with water and suspended in methylene chloride and the insoluble material is filtered off with suction. The filtrate is washed with saturated sodium chloride solution, dried over sodium sulphate and concentrated to give 19.2 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05596006 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-f1561e61898748a3a269f986c1bff134 |
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| Source note | uspto-grants-1997_01 |
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