HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440656Generated: October 29, 2026
N-bromobutanimide → 3-Bromo-4-chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran
https://huagongshe.com/reaction/440656
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran | HCID 22404776 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-Bromo-4-chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran | HCID 22404815 | 95.4% |
Reaction Steps
A mixture of 11.82 g (0.052 mole) of 4-chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran (Example 1, Step C) and 9.3 g (0.052 mole) of N-bromosuccinimide in 200 mL of carbon tetrachloride was irradiated with a sun lamp for approximately 16 hours. No reaction occurred during this time. To this mixture was then added 0.10 g of benzoyl peroxide, and the reaction mixture was then heated at reflux and irradiated simultaneously for a period of five hours. The sun lamp was turned off, and the mixture was allowed to stir while being heated at reflux for an additional hour. The mixture was then passed through a column of silica gel, and product-containing fractions were combined. The solvent was evaporated from the combined fractions under reduced pressure, leaving 15.2 g of 3-bromo-4-chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran as a solid, m.p. 103°-104° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05521147 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-e054de35a3e44bf4a04a6d695b45b00d |
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| Source note | uspto-grants-1996_05 |
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