HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 7-bromo-2,3-dihydro-1,4-benzodioxin-6-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1,4-Benzodioxan-6-ylamine | HCID 89148 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-bromo-2,3-dihydro-1,4-benzodioxin-6-amine | HCID 4983229 | 93% |
Reaction Steps
A solution of 2,3-dihydro-benzo[1,4]dioxin-6-ylamine (1 g, 6.6 mmol) in tetrahydrofuran (15 ml) was cooled to −78 deg C. then treated with 1 drop of concentrated sulphuric acid followed by N-bromosuccinimide (1.2 g, 6.6 mmol). The mixture was allowed to warm to room temperature over 1 hour then evaporated. The residue was dissolved in ether, washed with water then brine, dried and evaporated to afford an oil (1.4 g, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07498326B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-5389309b1db84247bd8965dc569dee38 |
| Source note | uspto-grants-2009_03 |