HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 4,7-dibromo-3,4-dihydrobenzo[b]oxepin-5(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 7-Bromo-3,4-dihydro-1-benzoxepin-5(2H)-one | HCID 10681548 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4,7-dibromo-3,4-dihydrobenzo[b]oxepin-5(2H)-one | HCID 57900458 | 91.9% |
Reaction Steps
To 7-bromo-3,4-dihydrobenzo[b]oxepin-5(2H)-one (3 g, 12 mmol) in ether (110 mL) was added bromine (0.7 mL, 14 mmol) and allowed to stir at room temperature overnight. The reaction mixture was concentrated under reduced pressure and purified via ISCO chromatography (hexane to 20% hexane in EtOAc over 45 minutes). Collected fractions and concentrated to give 4,7-dibromo-3,4-dihydrobenzo[b]oxepin-5(2H)-one (3.53 g, 89%). 1H NMR (500 MHz, CDCl3) δ 7.86 (d, J=2.5, 1H), 7.52 (dt, J=28.5, 14.2, 1H), 6.97 (d, J=8.7, 1H), 4.95 (dd, J=7.6, 6.8, 1H), 4.53-4.36 (m, 1H), 4.17 (ddd, J=12.8, 9.9, 4.4, 1H), 3.04-2.84 (m, 1H), 2.52 (ddt, J=14.7, 7.8, 4.5, 1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08242104B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-6cb706e200c444feb577f7de32a39f20 |
| Source note | uspto-grants-2012_08 |