HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335912Generated: October 30, 2026
Boron tribromide → HCID 58466135, compound
https://huagongshe.com/reaction/335912
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 59272305 | HCID 59272305 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58466135 | HCID 58466135 | — |
Reaction Steps
To a solution of 2′-bromo-1′-fluoro-7′-methoxy-5H-spiro[oxazole-4,9′-xanthen]-2-amine (0.575 g, 1.516 mmol) in 15 mL of CH2Cl2 at −15° C. was added boron tribromide (1.0 M in CH2Cl2, 4.55 mL, 4.55 mmol). The mixture was slowly allowed to warm to 0° C. over the course of 1.25 hours at which point the reaction was carefully quenched with 2 mL of MeOH and saturated sodium bicarbonate (100 mL). This mixture was poured into a separatory funnel containing EtOAc (100 mL). The layers were separated and the aqueous layer was extracted with EtOAc (2×100 mL). The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo to provide 2-amino-2′-bromo-1′-fluoro-5H-spiro[oxazole-4,9′-xanthen]-7′-ol as a glassy red solid. MS m/z=365.1 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883782B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-1cb1d0bdfeb8429f849515853cb48c3b |
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| Source note | uspto-grants-2014_11 |
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