HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium sulfate decahydrate → (1H-Indazol-7-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium sulfate decahydrate | HCID 62649 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl 1H-indazole-7-carboxylate | HCID 45790508 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1H-Indazol-7-yl)methanol | HCID 44119262 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
In a round-bottomed flask, ethyl 1H-indazole-7-carboxylate (600 mg, 3.15 mmol) was dissolved in THF (16 ml). The light yellow solution was cooled to 0° C. and lithium aluminum hydride (1.0 M in THF, 3.8 ml, 3.8 mmol) was added dropwise. The bright yellow reaction mixture was stirred at 0° C. for 1.25 h then sodium sulfate decahydrate was carefully added. When gas evolution had stopped, the ice bath was removed, sodium sulfate was added and the mixture was stirred for 30 min at room temperature. The suspension was filtered over Celite and rinsed with ethyl acetate/methanol. The filtrate was concentrated to afford (1H-indazol-7-yl)-methanol as a light yellow solid which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658646B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-46ef2a0ba2bc4954b97c02e7f082d5e2 |
| Source note | uspto-grants-2014_02 |