HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridiniumtribromide → 7-Bromo-5-isobutyl-3,3-dimethyl-2,3-dihydro-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridiniumtribromide | HCID 21124087 | — |
| Reactant | 5-Isobutyl-3,3-dimethyl-2,3-dihydro-benzofuran | HCID 22041397 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Bromo-5-isobutyl-3,3-dimethyl-2,3-dihydro-benzofuran | HCID 22041410 | 68.5% |
Reaction Steps
To a solution of 5-isobutyl-3,3-dimethyl-2,3-dihydro-benzofuran (1.59 g, 7.78 mmol) in dichloromethane (40 mL) was added pyridinium tribromide (2.49 g, 7.78 mmol) and the reaction mixture stirred at room temperature overnight. The solution was washed with water and brine, dried (MgSO4), filtered and evaporated. The residue was purified on silica gel (0% to 2% ethyl acetate in hexane) to give 1.51 g of 7-bromo-5-isobutyl-3,3-dimethyl-2,3-dihydro-benzofuran (68%). 1H NMR (300 MHz; CDCl3): δ 0.90 (d, J=6.3 Hz, 6H), 1.33 (s, 6H), 1.77 (m, 1H), 2.39 (d, J=7.5 Hz, 2H), 4.30 (s, 2H), 6.80 (d, J=1.5 Hz, 1H), 7.05 (d, J=1.5 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07196108B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-3ebd96619f584988882e4ef33576ddad |
| Source note | uspto-grants-2007_03 |