HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515224Generated: November 3, 2026
Boron trifluoride etherate → 2-Bromo-6H-dibenz[b,e]oxepin-11-one
https://huagongshe.com/reaction/1515224
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 2-(4-Bromophenoxymethyl)benzoic acid | HCID 10709836 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-6H-dibenz[b,e]oxepin-11-one | HCID 12929131 | 91.2% |
Reaction Steps
Trifluoroacetic anhydride (56.0 mL, 400 mmol) was added dropwise to a dichloromethane (500 mL) solution of 2-(4-bromophenoxymethyl)benzoic acid (112 g, 364 mmol) at room temperature. The mixture was stirred at room temperature for 2 hour, BF3.OEt2 (10 mL, 169.3 mmol) was then added thereto, and the mixture was stirred at room temperature for additional 2 hours. The reaction mixture was washed with a saturated aqueous sodium bicarbonate solution, and then with a saturated sodium chloride solution, the washed mixture was then dried over anhydrous sodium sulfate, and the solvents were distilled off under a reduce pressure. The residue was purified by column chromatography (hexane-ethyl acetate=3:2), to give 96.0 g (91%) of the captioned compound in the form of crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08222419B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-5f12d24f8ce84c31aa43db3ce0b61781 |
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| Source note | uspto-grants-2012_07 |
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