HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 21357383, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22993556 | HCID 22993556 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21357383 | HCID 21357383 | — |
Reaction Steps
To a solution of 1-(3-hydroxypropyl)-4-[pyrid-2-yl]pyridinium bromide (8 g) in 100 mL EtOH was added NaBH4 (1.41 g, 37.2 mmol) in small portions. The reaction mixture was stirred at room temperature for 12 h and then quenched with drops of water. The solvent was removed in vacuo and the residue was purified by column chromatography over silica gel with 1:4 MeOH/EtOAc followed by 1:4 (2M NH3 in MeOH)/EtOAc as the eluting system (Rf =0.6, (2M NH3 in MeOH)/EtOAc=1:4) to obtain 3-(3',6'-dihydro-2'-H-(2,4']bipyridinyl-1'-yl)-propanol as an oil (1.58 g, 39% over two steps).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06159990 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-4e34cd573df04cbcace335aebbf7055a |
| Source note | uspto-grants-2000_12 |