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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416510Generated: November 3, 2026

p-Toluenesulfonic acid → 4-(1,3,4-Oxadiazol-2-yl)benzaldehyde

https://huagongshe.com/reaction/2416510

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 22631214HCID 22631214—
SolventOxolane--water (1/1)HCID 21881883—
Product4-(1,3,4-Oxadiazol-2-yl)benzaldehydeHCID 2263086372%

Reaction Steps

To the product from step B (175 mg, 0.80 mmol) in a 1:1 mixture of tetrahydrofuran/water (2 mL) at room temperature was added p-toluenesulfonic acid (50 mg, 0.3 mmol). The reaction mixture was stirred at room temperature for 1 h, and partitioned between dichloromethane and sat. aq. NaHCO3. The organic layer was dried with Na2SO4, and concentrated in vacuo to give 100 mg (72%) of the title product, which was used without further purification. MS 175 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825170B2
Source datasetuspto-grants-2004_11
ORD IDord-f806d48a5f7f4ab3aaffcf3af5ca9584
Source noteuspto-grants-2004_11