Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 2,7-dibromo-9H-xanthen-9-one | HCID 363840 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Bromo-9-xanthenone | HCID 5068963 | 41% |
Reaction Steps
The reaction solution was refluxed for 5 hours at 100° C. under heating and stirring in a nitrogen atmosphere. Upon completion of the reaction, chloroform and a saturated aqueous sodium sulfite solution were added to the reaction solution and stirring was continued until the color of bromine was lost. The organic layer was separated, washed with a saturated aqueous sodium carbonate solution, dried with magnesium sulfate, and filtered. The solvent in the filtrate was distilled away at a reduced pressure. The precipitated solid was purified with a silica gel column (toluene: 100%). As a result, 2.9 g (yield: 41%) of 2-bromoxanthone and 2.2 (yield: 25%) g of 2,7-dibromoxanthone were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09269911B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-68c2f266db164b3796528f12cb1801e7 |
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| Source note | uspto-grants-2016_02 |
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