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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638547Generated: November 1, 2026

Triethylamine → 3-Cyclopropyl-5-(isocyanomethyl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/1638547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN-((3-Cyclopropyl-1,2,4-oxadiazol-5-yl)methyl)formamideHCID 14460538—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-Cyclopropyl-5-(isocyanomethyl)-1,2,4-oxadiazoleHCID 22912924—

Reaction Steps

A stirred solution of 3-cyclopropyl-5-formylaminomethyl-1,2,4-oxadiazole (60 mmol) and triethylamine (176 mmol) in CH2Cl2 (100 ml) was charged at 0° C. dropwise with POCl3 (60 mmol). The mixture was then left for 30 min. with stirring at 0° C., whereafter a solution of Na2CO3 (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 at 2160 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880799
Source datasetuspto-grants-1989_11
ORD IDord-786306c7e96c4dd08b23efe7ab987591
Source noteuspto-grants-1989_11