HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481331Generated: November 1, 2026
Azobisisobutyronitrile → 2-(Bromomethyl)-4,6-dichlorobenzonitrile
https://huagongshe.com/reaction/1481331
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,4-Dichloro-6-methylbenzonitrile | HCID 2800965 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 2-(Bromomethyl)-4,6-dichlorobenzonitrile | HCID 89704997 | — |
Reaction Steps
A solution of 2,4-dichloro-6-methylbenzonitrile (16.9 mmol) in 34 mL chlorobenzene was heated to 50° C. when NBS (18.6 mmol) was added. The flask was purged with Ar before AIBN (1.69 mmol) was added at once still at 50° C. The reaction mixture was then stirred at 78° C. After 2 h and 4 h, another portion of AIBN (1.69 mmol) was added and heating to 78° C. was continued overnight. The solvent was then evaporated off, the resulting residue was redissolved in Et2O and the remaining solid was removed by filtration. The filtrate was washed twice with 2N HCl solution and brine, it was dried over MgSO4 and concentrated in vacuo. Purification with CC (KP-SIL™ from Biotage) using Hept to EtOAc gives the desired compound as yellowish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409917B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-148fe8e8fe2845a5b253f11f21731bb7 |
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| Source note | uspto-grants-2016_08 |
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