HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505695Generated: October 26, 2026
Benzoyl Peroxide → 2-(Bromomethyl)-4-fluorobenzonitrile
https://huagongshe.com/reaction/505695
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Fluoro-2-methylbenzonitrile | HCID 3826055 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(Bromomethyl)-4-fluorobenzonitrile | HCID 21984990 | 25% |
Reaction Steps
A solution of 2-methyl-4-fluoro-benzonitrile (3.5 g, 25.9 mmol) in 40 mL of carbon tetrachloride was treated with N-Bromosuccinimide (4.6 g, 25.9 mmol) and benzoylperoxide (157 mg, 0.65 mmol). The mixture was heated to reflux for 3 hours, cooled to room temperature and allowed to stir overnight. The solids were filtered off and washed with carbon tetrachloride. The filtrate was condensed and purified by normal phase flash column chromatography on a 50 g silica gel column (5-50% ethyl acetate/hexanes gradient). Two peaks separated. It was determined that the second eluting peak is the desired product. Pure fractions of this peak were pooled and concentrated in vacuo to yield 2-(bromomethyl)-4-fluorobenzonitrile (1.35 g, 0.63 mmol, 25% yield) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 4.79 (s, 2H), 7.44 (dt, J=8.59, 2.69 Hz, 1H), 7.68 (dd, J=9.53, 2.55 Hz, 1H), 8.01 (dd, J=8.59, 5.64 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781428B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-15e7e22a8e164223882fa189072229dc |
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| Source note | uspto-grants-2010_08 |
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