HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335910Generated: October 26, 2026
2-bromo-3,5-difluoro-7-methoxy-9H-xanthen-9-one → 2-bromo-3,5-difluoro-7-methoxy-9-methyl-9H-xanthen-9-ol
https://huagongshe.com/reaction/335910
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-bromo-3,5-difluoro-7-methoxy-9H-xanthen-9-one | HCID 67382909 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-bromo-3,5-difluoro-7-methoxy-9-methyl-9H-xanthen-9-ol | HCID 67383546 | — |
Reaction Steps
A mixture of 2-bromo-3,5-difluoro-7-methoxy-9H-xanthen-9-one (40 g, 117 mmol) and THF (300 mL) was cooled to 0° C. and treated with methylmagnesium chloride (58.6 mL, 176 mmol) (3M in THF). After stirring at this temperature for 20 minutes, the reaction was quenched by the addition of sataturated NH4Cl (500 mL). Brine was added and the mixture was extracted with EtOAc (3×100 mL). The combined organic extracts were dried with sodium sulfate, filtered and concentrated in vacuo to afford crude 2-bromo-3,5-difluoro-7-methoxy-9-methyl-9H-xanthen-9-ol as a brown solid that was carried on without further purification. MS m/z=339.0 [M+1−H2O].
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-6d31548d0ce94dba926180b1dce661c8 |
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| Source note | uspto-grants-2014_11 |
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