HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(6-Bromopyridin-2-yl)-2-fluoroethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(6-Bromopyridin-2-yl)-2-fluoroethanone | HCID 59526299 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(6-Bromopyridin-2-yl)-2-fluoroethanol | HCID 59525900 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
1-(6-Bromopyridin-2-yl)-2-fluoroethanone (0.53 g, 2.43 mmol) was taken up in MeOH (12 mL) and cooled to 0° C. Sodium borohydride (0.092 g, 2.43 mmol) was added and the mixture stirred at 0° C. for 1 hour. Water was added and the reaction mixture was extracted with EtOAc (2×). The combined organic extracts were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo to give the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367706B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-4aefd070f3b14724a55454cedad94b40 |
| Source note | uspto-grants-2013_02 |