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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741145Generated: October 26, 2026

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

https://huagongshe.com/reaction/1741145

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 2179386096.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred mixture of naphthalene-2-carboxylic acid hydrazide (2.0 g, 10.7 mmol, prepared 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 numberUS05972978
Source datasetuspto-grants-1999_10
ORD IDord-14d2634398e149b59fbd5cc57890b9d6
Source noteuspto-grants-1999_10