HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisobutylaluminum hydride → (6-Chloro-5-methylpyridin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Methyl 6-chloro-5-methylpyridine-3-carboxylate | HCID 12404031 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (6-Chloro-5-methylpyridin-3-yl)methanol | HCID 11686949 | 88.3% |
Reaction Steps
To a solution of methyl 6-chloro-5-methyl-3-pyridinecarboxylate (84 mg, 0.453 mmol) in DCM (2 ml), DIBAL-H (1.5 M solution in toluene, 0.905 ml, 1.358 mmol) was added dropwise under N2 at −78° C. The reaction mixture was allowed to attain rt and stirred overnight. After 18 h, TLC showed no starting material. The reaction was quenched by addition of sodium-potassium tartrate saturated solution, extracted with DCM, dried, filtered, and concentrated to afford (6-chloro-5-methyl-3-pyridinyl)methanol (63 mg, 0.400 mmol, 88% yield) pure enough to be used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08097628B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-897fb46fdb5f43529eb7c167b8c301fe |
| Source note | uspto-grants-2012_01 |