HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335915Generated: October 25, 2026
7-bromo-4-fluoro-2-methoxy-9H-xanthen-9-one → 7-bromo-4-fluoro-2-methoxy-9-methyl-9H-xanthen-9-ol
https://huagongshe.com/reaction/335915
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 7-bromo-4-fluoro-2-methoxy-9H-xanthen-9-one | HCID 57475639 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-bromo-4-fluoro-2-methoxy-9-methyl-9H-xanthen-9-ol | HCID 67382921 | — |
Reaction Steps
7-bromo-4-fluoro-2-methoxy-9H-xanthen-9-one (22 g, 68.1 mmol) was dissolved in 300 ml of THF and cooled to −30° C. in a dry ice ACN bath. Methylmagnesium chloride (34.0 mL, 102 mmol) (3M in THF) was added to the slurry maintaining temperature less than −15° C. The solution was allowed to warm to RT (undissolved solids went into solution), then quenched with saturated NH4Cl (250 mL). The aqueous layer was extracted with EtOAc (3×200 mL) and the combined organic layers were washed with brine and dried over anhydrous sodium sulfate, filtered and concentrated to afford 7-bromo-4-fluoro-2-methoxy-9-methyl-9H-xanthen-9-ol as a brown liquid that was used without further purification.
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-6a8d8e9f9362467796036fcc222f81eb |
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| Source note | uspto-grants-2014_11 |
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