HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176033Generated: October 31, 2026
N-bromobutanimide → Benzyl 5-(bromomethyl)thiophene-2-carboxylate
https://huagongshe.com/reaction/2176033
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 90370165 | HCID 90370165 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Benzyl 5-(bromomethyl)thiophene-2-carboxylate | HCID 89534603 | 62.9% |
Reaction Steps
To a mixture of 5.27 g of benzyl 5-methylthiophene-2-carboxylate and 100 mL of carbon tetrachloride were added 4.18 g of N-bromosuccinimide (NBS) and 142 mg of azobisisobutyronitrile (AIBN), followed by stirring overnight at 80° C. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=7:3), thereby obtaining 4.44 g of benzyl 5-(bromomethyl)thiophene-2-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062032B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-da8b347f497b44869d766cffe3a42206 |
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| Source note | uspto-grants-2015_06 |
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