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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576864Generated: October 29, 2026

2-Thiophenecarboxaldehyde → Benzoxazole, 5-nitro-2-(2-thienyl)-

https://huagongshe.com/reaction/1576864

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ThiophenecarboxaldehydeHCID 7364—
Reactant2-Amino-4-NitrophenolHCID 3613389—
ReactantHCID 178418268HCID 178418268—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductBenzoxazole, 5-nitro-2-(2-thienyl)-HCID 1125362150.4%

Reaction Steps

15.4 g of 4-nitro-o-aminophenol and 11.2 g of thiophenecarboxaldehyde are dissolved in glacial acetic acid (450 ml) and heated to 85°. 44.4 g of lead tetraacetate is dissolved in 400 ml glacial acetic acid by warming and added to the above solution. Heating is continued for 0.5 hr and the solution is cooled to room temperature, diluted with an equal volume of water and the dark precipitate is collected and washed with additional water. The crude product is dissolved in CH2Cl2 (800 ml) and heated with 2.0 g of "Darco" G-60, followed by evaporation of the CH2Cl2. The resulting material is recrystallized from ethanol-chloroform (3:1) to yield 12.4 g of 5-nitro-2-(2-thienyl)benzoxazole, mp 186°-188°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03983130
Source datasetuspto-grants-1976_09
ORD IDord-cf6536ab87f64c919ff653a780633f6d
Source noteuspto-grants-1976_09