HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091595Generated: November 1, 2026
Methanesulfonic Acid → 8-bromo-3,4-dihydrobenzo[f][1,4]oxazepin-5(2H)-one
https://huagongshe.com/reaction/2091595
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 7-bromo-3,4-dihydro-2H-1-benzopyran-4-one | HCID 22335736 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-bromo-3,4-dihydrobenzo[f][1,4]oxazepin-5(2H)-one | HCID 70655165 | 101.9% |
Reaction Steps
A solution of 7-bromochroman-4-one (340 mg, 1.5 mmol) and methanesulfonic acid (3 mL, 23.0 mmol) in DCM was cooled to 0° C. and treated with NaN3 (146 mg, 2.25 mmol) portionwise, while maintaining the internal temperature below 5° C. The reaction was then stirred at 0° C. for 4 h. At completion, the reaction was slowly neutralized with 8 N aq. NaOH, then diluted with DCM (20 mL) and water (20 mL). The layers were separated and the organics were dried over MgSO4, filtered and evaporated to afford 8-bromo-3,4-dihydrobenzo[f][1,4]oxazepin-5(2H)-one (370 mg, 100% yield). MS (EI) m/z=242.1 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440652B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-00920c737cf641ca9f476fbbc8681774 |
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| Source note | uspto-grants-2013_05 |
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