HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717190Generated: October 25, 2026
Hydrogen Bromide → 4-Bromo-2-fluoro-3-methylbenzonitrile
https://huagongshe.com/reaction/717190
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium nitrite | HCID 516910 | — |
| Reactant | 4-Amino-2-fluoro-3-methylbenzonitrile | HCID 45078676 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Bromo-2-fluoro-3-methylbenzonitrile | HCID 59556913 | 80% |
Reaction Steps
A mixture of dimethyl sulfoxide (400 mL) and potassium nitrite (22.67 g, 266 mmol) was stirred to dissolve potassium nitrite and 4-amino-2-fluoro-3-methylbenzonitrile (10 g, 66.6 mmol) and copper(I) bromide (1.911 g, 13.32 mmol) were added. Aqueous 48% hydrogen bromide (33 mL, 266 mmol), diluted with dimethyl sulfoxide (200 mL), was added dropwise and the reaction stirred for 2 h. After complete conversion of starting material, the reaction mixture was poured into iced-cold water and neutralized to pH 7 with cold concentrated sodium hydroxide. The resulting solid was collected by filtration to give the desired product (11.4 g, 53.3 mmol, 80% yield) as white solid. 1H NMR (400 MHz, CHLOROFORM-d) δ (ppm) 7.47 (d, J=9.37 Hz, 1H), 7.33 (t, 1H), 2.39 (d, J=2.34 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193692B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-7d6b1d4bcca846e3a034e199c25559e6 |
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| Source note | uspto-grants-2015_11 |
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