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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421918Generated: October 27, 2026

Triethylamine → 5-Naphthalen-2-yl-3H-[1,3,4]oxadiazol-2-one

https://huagongshe.com/reaction/1421918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-NaphthohydrazideHCID 123485—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
SolventTetrahydrofuranHCID 8028—
Product5-Naphthalen-2-yl-3H-[1,3,4]oxadiazol-2-oneHCID 21793860—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred mixture of naphthalene-2-carboxylic acid hydrazide (2.0 g, 10.7 mmol, pre pared as described in example 1) and triethylamine (1.1 g, 10.7 mmol) in dry tetrahydrofuran (40 ml) was added carbonyl diimidazole (2.2 g, 13.4 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 1 h and at room temperature for 17 h. The resulting reaction mixture was evaporated in vacuo and to the residue was added water (50 ml) and ethyl acetate (50 ml). The phases were separated and the organic phase was washed with saturated aqueous sodium chloride (2×25 ml), dried (MgSO4) and filtered and evaporated in vacuo affording 2.2 g of crude product which was recrystallised from a mixture of ethyl acetate and heptane 1:1 (60 ml) affording after drying in vacuo at 50° C. 1.2 g (52%) of the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080770
Source datasetuspto-grants-2000_06
ORD IDord-46a6fb7277624343960915c9002c16dc
Source noteuspto-grants-2000_06