HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → (3-Chloropyridin-4-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-Chloro-4-pyridinecarboxaldehyde | HCID 2762995 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | (3-Chloropyridin-4-yl)methanol | HCID 12742466 | 90.2% |
Reaction Steps
To a mixture of 1.53 g of 3-chloroisonicotinaldehyde and 5 ml of ethanol was gradually added 0.40 g of sodium borohydride under ice-cooling, and the mixture was stirred under ice-cooling for 1 hour, and subsequently at room temperature for 1 hour. Saturated brine was added to the reaction mixture, and the mixture was extracted twice with ethyl acetate. The organic layers were combined and dried over magnesium sulfate. The resulting mixture was concentrated under reduced pressure to obtain 1.40 g of (3-chloropyridin-4-yl)methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08796306B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-1cfaa679637c436e9665911fc57648dd |
| Source note | uspto-grants-2014_08 |