HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 5-bromo-3,3-dimethyl-2,3-dihydro-1H-indol-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 3,3-Dimethyl-1,3-dihydro-indol-2-one | HCID 313100 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-bromo-3,3-dimethyl-2,3-dihydro-1H-indol-2-one | HCID 12052796 | — |
Reaction Steps
3,3-Dimethyl-1,3-dihydro-2H-indol-2-one (1.12 g, 6.95 mmol) was dissolved in chloroform and stirred at room temperature under nitrogen. Bromine (1.12 g) was added and the mixture was heated under reflux until HBr evolution ceased and the bromine colour was discharged from the solution. The solution was washed with sodium metabisulphite solution and sodium hydrogen carbonate solution, dried (MgSO4), filtered and concentrated to dry under reduced pressure to give 5-bromo-3,3-dimethyl-1,3-dihydro-2H-indol-2-one as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05773448 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-fcac48bae2a64d0fa2b020fa59c1c363 |
| Source note | uspto-grants-1998_06 |