HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Piperidinemethanol → HCID 52234807, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Piperidinemethanol | HCID 420771 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3-Phenyl-1,2-oxazole-5-carbaldehyde | HCID 11367267 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 52234807 | HCID 52234807 | 102.4% |
Reaction Steps
Sodium triacetoxyborohydride (12.2 g) was added portionwise to a room temperature mixture of the compound prepared in Example 7 (5.00 g) and piperidin-4-ylmethanol (4.99 g) in dichloromethane (150 mL). The reaction mixture was stirred at room temperature overnight. The reaction mixture was diluted with dichloromethane and washed sequentially with a saturated aqueous sodium bicarbonate solution and brine. The organics were dried over anhydrous magnesium sulfate and concentrated to obtain the crude title compound (8.05 g), which was used without further purification having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08809538B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-ac4271aac7e448568fa0134caf35d304 |
| Source note | uspto-grants-2014_08 |