HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanol → methyl 1-cyclohexyl-1H-indazole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | methyl 1H-indazole-3-carboxylate | HCID 657476 | — |
| Reactant | Diethylazodicarboxylate toluene | HCID 66777355 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl 1-cyclohexyl-1H-indazole-3-carboxylate | HCID 66778143 | 93% |
Reaction Steps
To a mixture of methyl 1H-indazole-3-carboxylate (5.00 g), cyclohexanol (9.00 mL), triphenylphosphine (14.9 g) and tetrahydrofuran (100 mL) was added 40% diethyl azodicarboxylate toluene solution (25.6 mL), and the mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure, diethyl ether was added to the residue, and the mixture was stirred at 0° C. The precipitate was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:9, volume ratio) to give the title object compound (6.84 g, 93%) as a pale-red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436043B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-86826ed234a046229b5877ca30ddfe44 |
| Source note | uspto-grants-2013_05 |