HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508176Generated: October 31, 2026
Hydrogen Bromide → 3-Bromo-2,6-dichlorobenzonitrile
https://huagongshe.com/reaction/1508176
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Amino-2,6-dichlorobenzonitrile | HCID 15405299 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Bromo-2,6-dichlorobenzonitrile | HCID 71239371 | — |
Reaction Steps
To 1 mL of conc. H2SO4 was portionwise added sodium nitrite (1.38 mmol). After complete dissolution, a solution of 3-amino-2,6-dichlorobenzonitrile (1.24 mmol) in 2.5 mL glacial acetic acid was added at 0° C. After 30 min at 0° C., a precooled solution of CuBr (2.76 mmol) in 0.5 mL HBr (48% in H2O) was slowly added. The reaction was stirred at 0° C. for 45 min and then at RT for 45 min. The mixture was quenched with water and extracted with EtOAc (3×). The combined organic layers were washed with brine, dried over MgSO4 and concentrated in vacuo to give the desired product as brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221832B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-dd4ee12fbcb24b63a764c221090ab5b3 |
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| Source note | uspto-grants-2015_12 |
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