HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427908Generated: November 2, 2026
Azobisisobutyronitrile → 4-(bromomethyl)-5-chloro-2-fluoro-N-(methylsulfonyl)benzamide
https://huagongshe.com/reaction/1427908
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Chloro-2-fluoro-4-methyl-N-(methylsulfonyl)benzamide | HCID 58042368 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-(bromomethyl)-5-chloro-2-fluoro-N-(methylsulfonyl)benzamide | HCID 58042397 | — |
Reaction Steps
A mixture of 5-chloro-2-fluoro-4-methyl-N-(methylsulfonyl)benzamide (0.8 g, 3.0 mmol), N-bromosuccinimide (1.6 g, 9.0 mmol) and azodiisobutyronitrile (16 mg, 0.09 mmol) in 1,2-dichloroethane (20 mL) was stirred at 90° C. for 16 hrs. The reaction was quenched with Na2S2O3 (10 mL, 10%), extracted with 1,2-dichloroethane (20 mL×3), dried over anhydrous Na2SO4, concentrated and the residue was used in next step without further purification (1.1 g, crude). LCMS (ESI) m/z: 342.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933236B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-4dfbde27ee814d9286f78d95ecb4ef28 |
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| Source note | uspto-grants-2015_01 |
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