HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226008Generated: October 27, 2026
N-bromobutanimide → 2-Bromo-5-fluoro-3-methylbenzo[b]thiophene
https://huagongshe.com/reaction/226008
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Fluoro-3-methyl-benzo[b]thiophene | HCID 596828 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Bromo-5-fluoro-3-methylbenzo[b]thiophene | HCID 66721202 | — |
Reaction Steps
A mechanically-stirred solution of 5-fluoro-3-methylbenzo[b]thiophene (50.32 g, 0.303 mol, 1.0 equiv) in acetonitrile (350 mL) is treated with NBS (56.32 g, 0.318 mol, 1.05 equiv). An initial endotherm reduces the reaction temperature to 17° C. A subsequent exotherm then increases the reaction temperature to 40° C. over a 10 min. period, at which time the reaction is cooled to 18-20° C. by application of an ice water bath. The reaction is stirred at RT for an additional 35 min. and the resultant slurry is slowly diluted with water (350 mL). The slurry is stirred for 10 min and the product is filtered, washed with 50:50 acetonitrile:water (100 mL) and dried to a colorless crystalline solid (65.56 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557103B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-d7980c324e7e437d8e60bd8c7dc6666b |
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| Source note | uspto-grants-2009_07 |
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