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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291267Generated: October 30, 2026

Triethylamine → 1,2,4-Oxadiazole, 5-cyclopropyl-3-(isocyanomethyl)-

https://huagongshe.com/reaction/2291267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant5-Cyclopropyl-3-formylamino-methyl1,2,4-oxadiazoleHCID 86741100—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1,2,4-Oxadiazole, 5-cyclopropyl-3-(isocyanomethyl)-HCID 10749342—

Reaction Steps

A stirred solution of 5-cyclopropyl-3-formylamino-methyl-1,2,4-oxadiazole (60 mmol) and triethylamine (176 mmol) in CH2Cl2 (100 ml) was charged dropwise with POCl3 (60 mmol) at 0° C. The mixture was then left for 30 minutes with stirring at 0° C., whereafter a solution of 60 mmol) in H2O (50 ml) was added. The mixture was heated to room temperature, whereafter the organic phase was separated, dried and evaporated in vacuo. The residue was treated with ether, decanted and the solution was evaporated to give the title compound as an oil. The oil was processed without any further purification. The compound was characterized by its IR absorbtion band at 2160 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04795749
Source datasetuspto-grants-1989_01
ORD IDord-515aba5a36724bcc921f57a49355222a
Source noteuspto-grants-1989_01