HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 4-(bromoacetyl)-7-methyl-2H-chromen-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-(1-ethoxyvinyl)-7-methyl-2H-chromen-2-one | HCID 59774894 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | 4-(bromoacetyl)-7-methyl-2H-chromen-2-one | HCID 86621974 | — |
Reaction Steps
To a solution of 4-(1-ethoxyvinyl)-7-methyl-2H-chromen-2-one (1.56 g, 6.77 mmol) in THF-water (27.5 mL, 10/1 mixture), N-bromosuccinimide (1.33 g, 7.45 mmol) was added. The reaction was then stirred at room temperature. After 3 hours stirring, toluene was added and the crude mixture was evaporated under reduced pressure. The crude residue obtained was purified by column chromatography (EtOAc/hexanes, 30:70) to afford the title compound. 1H NMR (400 MHz, acetone-d6): 7.71 (d, 1H), 7.24 (s, 1H), 7.22 (d, 1H), 6.94 (s, 1H), 4.90 (s, 2H), 2.50 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07960409B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-17c3b63a53fa4b75aed1ba06f33ac336 |
| Source note | uspto-grants-2011_06 |