HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912474Generated: October 26, 2026
Tetrahydrofuran → 1-(6-bromo-5-(2,4-difluorophenoxy)-1H-indazol-1-yl)-2-methylpropan-2-ol
https://huagongshe.com/reaction/912474
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-(6-Bromo-5-(2,4-difluorophenoxy)-1H-indazol-1-yl)propan-2-one | HCID 67416879 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(6-bromo-5-(2,4-difluorophenoxy)-1H-indazol-1-yl)-2-methylpropan-2-ol | HCID 67416478 | 96% |
Reaction Steps
To a stirred solution of 1-(6-Bromo-5-(2,4-difluorophenoxy)-1H-indazol-1-yl)propan-2-one (3.81 g, 10.0 mmol) in toluene (100 mL) at 21° C. was added a 3.0 M solution of methylmagnesium chloride in THF (5.0 mL, 15 mmol) in one portion. The temperature of the resulting solution rose to 34° C. and was stirred without any temperature control. After a total of 60 min the reaction mixture was quenched by addition of saturated ammonium chloride (50 mL). The resulting mixture was vigorously stirred for 20 min, then transferred to a separatory funnel and shaken. The organic layer was dried over sodium sulfate and the solvent removed under reduced pressure to afford the title compound as an orange oil (3.79 g, 96%) that slowly crystallized on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08026233B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-592930c06be24d70b616f07817898905 |
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| Source note | uspto-grants-2011_09 |
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