HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757079Generated: October 28, 2026
Hydrogen Bromide → 2-Bromo-4-methyl-5-nitroanisole
https://huagongshe.com/reaction/1757079
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Benzenamine, 2-methoxy-5-methyl-4-nitro- | HCID 67253 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-4-methyl-5-nitroanisole | HCID 284744 | — |
Reaction Steps
a mixture of 2-methoxy-5-methyl-4-nitroaniline (20 g, 110 mmol) in 140 mL of water was heated under reflux and 48% hydrobromic acid (56 mL) was added dropwise and the mixture was heated for 20 minutes. The resulting suspension was cooled to 0° C. and treated with 40 mL of aqueous sodium nitrite (7.6 g, 110 mmol) dropwise keeping the temperature at 0° C. The suspension was added carefully dropwise to a 0° C. solution of cuprous bromide (18.1 g, 126 mmol) in 96 mL of water and 38 mL of 48% HBr. The mixture was stirred at 0° C. for 30 minutes and at room temperature for 1 hour and finally on a steam bath for 20 minutes to complete the reaction. The solid precipitate was suction filtered and dissolved in methylene chloride, washed with 400 mL of 10% sodium hydroxide, 5% sodium bisulfite, and water. The organic layer was dried, filtered, and evaporated in vacuo to give 24.9 g of dark brown solid. This was recrystallized from hexane to give 13.4 g of bromo compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05444038 |
|---|
| Source dataset | uspto-grants-1995_08 |
|---|
| ORD ID | ord-5461b0259273488db663aef9c7548965 |
|---|
| Source note | uspto-grants-1995_08 |
|---|