Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454331Generated: October 29, 2026

Tetrapropylammonium → 3-[4-(Formyl)phenyl]-5-(4-phenyl-5-trifluoromethyl-2-thienyl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/1454331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrapropylammoniumHCID 9559—
ReactantMethyl morpholine oxideHCID 82029—
Reactant3-[4-(Hydroxymethyl)phenyl]-5-(4-phenyl-5-trifluoromethyl-2-thienyl)-1,2,4-oxadiazoleHCID 11153879—
SolventAcetonitrileHCID 6342—
Product3-[4-(Formyl)phenyl]-5-(4-phenyl-5-trifluoromethyl-2-thienyl)-1,2,4-oxadiazoleHCID 1121173666.5%

Reaction Steps

A mixture of 310 mg (0.77 mmol) of 3-[4-(hydroxymethyl)phenyl]-5-(4-phenyl-5-trifluoromethyl-2-thienyl)-1,2,4-oxadiazole (from Step E), 527 mg (1.5 mmol) of 4-methylmorpholine N-oxide and 500 mg of 4 A molecular sieves in 15 mL of CH3CN was treated with 12 mg (0.034 mmol) of tetrapropylammonium perruthnate and the resulting mixture was stirred ar rt for 2 h. The solids were filtered and the filtrated was concentrated. Chromatography on a Biotage 40 S cartridge using 9:1 v/v hexanes/EtOAc (1L) as the eluant afforded 205 mg (66%) of the title compound: 1H NMR (500 Mhz) δ 7.48 (app s, 5H), 7.93 (app s, 1H), 8.03 (d, J=8.5, 2H), 8.33 (d, J=8.5, 2H), 10.1 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07479504B2
Source datasetuspto-grants-2009_01
ORD IDord-3a81541e8974438c8d3768b654cd89c3
Source noteuspto-grants-2009_01