Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097677Generated: October 25, 2026

p-Toluenesulfonic acid → 3-[5-(Phenylmethyl)-1,2,4-oxadiazol-3-yl]propanal

https://huagongshe.com/reaction/1097677

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3-[3,3-Bis(ethyloxy)propyl]-5-(phenylmethyl)-1,2,4-oxadiazoleHCID 66812952—
SolventEthanolHCID 702—
Product3-[5-(Phenylmethyl)-1,2,4-oxadiazol-3-yl]propanalHCID 8664311389.9%

Reaction Steps

Crude 3-[3,3-bis(ethyloxy)propyl]-5-(phenylmethyl)-1,2,4-oxadiazole (5.63 g, 19.4 mmol) in EtOH (75 ml) was stirred with p-toluenesulphonic acid (0.738 g, 3.9 mmol) for 21 h and the mixture partitioned between EtOAc and water. The organics were isolated washed with water and brine, dried and concentrated to a red oil. This material contained significant amounts of acetal, therefore the oil was dissolved in THF (15 ml) and treated with 2M HCl solution for 2 h then partitioned between EtOAc and water. The organics were isolated washed with brine, dried and concentrated to yield 3-[5-(phenylmethyl)-1,2,4-oxadiazol-3-yl]propanal as a red/brown oil (3.77 g) which was used crude in the next stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143264B2
Source datasetuspto-grants-2012_03
ORD IDord-0cd3cb331f5641daa9cc2fb8ba8eadb5
Source noteuspto-grants-2012_03