HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-bromo-5-methoxy-2,3-dihydro-1H-inden-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Methoxyindan-1-one | HCID 78787 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-bromo-5-methoxy-2,3-dihydro-1H-inden-1-one | HCID 37818987 | — |
Reaction Steps
5-Methoxy-indane-1-one (17.2 g, 106.05 mmol) is suspended in 100 mL of water. The flask is covered with an aluminium foil to create a dark environment. N-Bromo-succinimide (18.87 g, 106.05 mmol) is added portionwise and the reaction mixture is stirred at room temperature overnight. The reaction mixture is extracted with 200 mL of ethyl acetate, the organic phase is collected, dried over sodium sulfate and concentrated under vacuum. The crude product obtained (20 g) is used in the next step without any further treatment.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633182B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-cba5939f0b054985826a413ac0332291 |
| Source note | uspto-grants-2014_01 |