HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77480Generated: October 29, 2026
Toluene → 1-(tetrahydro-2H-pyran-2-yl)-5-vinyl-1H-indazole
https://huagongshe.com/reaction/77480
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-bromo-1-(oxan-2-yl)-1H-indazole | HCID 53433826 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(tetrahydro-2H-pyran-2-yl)-5-vinyl-1H-indazole | HCID 86679770 | 74% |
Reaction Steps
To a solution of 5-bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (0.5 g, 1.778 mmol) in toluene (10 mL) and water (10 mL) were added K2CO3 (0.492 g, 3.56 mmol), trivinylboroxin pyridine complex (0.514 g, 2.134 mmol), and Tetrakis (0.206 g, 0.178 mmol). The reaction mixture was heated at 110° C. for 4 h. The reaction mixture was concentrated and the residue was extracted with ethyl acetate and washed with water. The organic layer was dried over anhydrous sodium sulfate and concentrated to give 1-(tetrahydro-2H-pyran-2-yl)-5-vinyl-1H-indazole (0.3 g, 74%). LCMS (ES-API), m/z 144 (M-THP).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841301B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-a29caa52d9d24a1a98c3b41fcb7a1a1b |
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| Source note | uspto-grants-2014_09 |
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