Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 21520276 | HCID 21520276 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 21520278 | HCID 21520278 | — |
Reaction Steps
28.0 g of recrystallized N-bromosuccinimide were added to a solution of 32.5 g of 7-ethyl-2-(2-methyl-1,3-dioxolan-2-yl)benzofuran in 480 ml of carbon tetrachloride. The resulting suspension was stirred and heated under reflux for 12 hours. The mixture was cooled overnight at 0°C, precipitated succinimide was filtered off and the filtrate was evaporated at 30°C under reduced pressure. There was thus obtained crude 7-(1'-bromoethyl)-2-(2-methyl-1,3-dioxolan-2-yl) benzofuran which was used immediately in the next stage. The structure of this compound was confirmed by spectral data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03972900 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-89321039a3d14ea28719b7e82301cda5 |
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| Source note | uspto-grants-1976_08 |
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