HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 3-[5-(Phenylmethyl)-1,2,4-oxadiazol-3-yl]-1-propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-[5-(Phenylmethyl)-1,2,4-oxadiazol-3-yl]propanal | HCID 86643113 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-[5-(Phenylmethyl)-1,2,4-oxadiazol-3-yl]-1-propanol | HCID 59395802 | 59% |
Reaction Steps
A solution of crude 3-[5-(phenylmethyl)-1,2,4-oxadiazol-3-yl]propanal (3.76 g, 17.4 mmol) in MeOH (60 ml) was cooled to 0° C. and sodium borohydride (0.724 g, 19.1 mmol) added portionwise over 30 min. The cooling bath was removed and the solution stirred for a further 1 h then partitioned between 1M HCl and EtOAc. The organic layer was separated and the aqueous extracted with EtOAc. The combined extracts were washed with brine, dried and concentrated to an orange liquid. This was purified on a 50 g silica SPE eluting with cyclohexane/EtOAc (20% to 80% gradient elution) to provide the title compound as a yellow oil (2.24 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143264B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-1849eeb0e6884b41835449b03b4ddc8b |
| Source note | uspto-grants-2012_03 |