HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-(propan-2-yl)pyridine-3-carboxylate → (2-Isopropylpyridin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-(propan-2-yl)pyridine-3-carboxylate | HCID 19690961 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Isopropylpyridin-3-yl)methanol | HCID 19691012 | — |
Reaction Steps
The 2-isopropyl-3-carboethoxypyridine (400 mg, 2 mmol) in distilled THF (50 mL) under nitrogen was cooled to 0° C. and lithium aluminum hydride (1M in THF) (2.07 mL) was added dropwise. The reaction was stirred for 18 hours at room temperature then cooled to 0° C. and quenched with EtOAc (100 μL), then H2O (100 μL), then 15% NaOH (100 μL), followed by H2O (300 μL). The mixture was filtered and the solvent was removed under reduced pressure. Toluene was added and the solvent was removed under reduced pressure to give the desired 2-isopropyl-3-hydroxymethylpyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05726172 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-13eeac45e3ff4344b45ee3f41e200838 |
| Source note | uspto-grants-1998_03 |