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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097678Generated: October 25, 2026

Sodium borohydride → 3-[5-(Phenylmethyl)-1,2,4-oxadiazol-3-yl]-1-propanol

https://huagongshe.com/reaction/1097678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-[5-(Phenylmethyl)-1,2,4-oxadiazol-3-yl]propanalHCID 86643113—
SolventMethanolHCID 887—
Product3-[5-(Phenylmethyl)-1,2,4-oxadiazol-3-yl]-1-propanolHCID 5939580259%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143264B2
Source datasetuspto-grants-2012_03
ORD IDord-1849eeb0e6884b41835449b03b4ddc8b
Source noteuspto-grants-2012_03