HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404193Generated: October 30, 2026
Azobisisobutyronitrile → 3-(Bromomethyl)-2-fluorobenzonitrile
https://huagongshe.com/reaction/404193
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Fluoro-3-methylbenzonitrile | HCID 23160359 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 3-(Bromomethyl)-2-fluorobenzonitrile | HCID 66678465 | — |
Reaction Steps
To a stirred solution of 2-fluoro-3-methylbenzonitrile (200 mg, 1.5 mmol) in 1,2-dichloroethane (30 ml) was added NBS (266 mg, 1.49 mmol) and AIBN (29 mg, 0.15 mmol) at RT. The reaction mixture was then heated to 80° C., and the reaction mixture was stirred for 2 h. After complete consumption of the starting material (by TLC), the reaction mixture was cooled to RT. The volatiles were removed under reduced pressure to obtain the crude material. Purification by silica gel column chromatography eluting with 2-3% EtOAc/hexane afforded compound I-6 (250 mg, 1.15 mmol, 78%) as colorless liquid. 1H NMR (500 MHz, CDCl3): δ 7.69-7.65 (m, 1H), 7.62-7.58 (m, 1H), 7.28-7.25 (m, 1H), 4.50 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748461B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-e3c7dd3f39684600ae0a99cba126c010 |
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| Source note | uspto-grants-2014_06 |
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