HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (2,6-Dichloro-3-hydroxymethyl-pyridin-4-yl)-pyrrolidin-1-yl-methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2,6-Dichloro-4-(pyrrolidine-1-carbonyl)-pyridine-3-carbaldehyde | HCID 86593985 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (2,6-Dichloro-3-hydroxymethyl-pyridin-4-yl)-pyrrolidin-1-yl-methanone | HCID 59678084 | — |
Reaction Steps
A mixture of the above aldehyde and sodium borohydride (400 mg, 10 mmol) in EtOH (50 mL) is stirred at room temperature for 1 hour. After evaporation of EtOH, EtOAc (40 mL) and water (40 mL) are added to the residue. The organic layer is separated, washed once with 1 N NaOH, 1N HCl and brine, dried (Na2SO4) and concentrated. The residue is chromatographed on silica gel (1:1 hexane:EtOAc) to give (2,6-dichloro-3-hydroxymethyl-pyridin-4-yl)-pyrrolidin-1-yl-methanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07342115B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-ea2e78f9821e4ed48f0d73071e11677c |
| Source note | uspto-grants-2008_03 |