HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186998Generated: November 2, 2026
N-bromobutanimide → 3-Bromo-6-fluoro-2-methylbenzonitrile
https://huagongshe.com/reaction/1186998
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Fluoro-6-methylbenzonitrile | HCID 18677151 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 3-Bromo-6-fluoro-2-methylbenzonitrile | HCID 66643852 | — |
Reaction Steps
To a cooled (0° C.) solution of 2-fluoro-6-methylbenzonitrile (5.0 g, 37 mmol) in 100 mL of concentrated H2SO4 was added NBS (6.93 g, 38.9 mmol). Then the mixture was stirred at 0° C. for 3 hrs and poured into ice-water (1 L). The solution was extracted three times with EtOAc (200 mL) and the combined organic layers were washed with water and brine, dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by silica gel flash chromatography to give 3-bromo-6-fluoro-2-methylbenzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673920B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-5cfb2e0c5b854581b10ad8f201b5d1a7 |
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| Source note | uspto-grants-2014_03 |
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