HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247119Generated: October 25, 2026
Cyanoacetic acid → 3-Chloromethyl-5-cyanomethyl-1,2,4-oxadiazole
https://huagongshe.com/reaction/247119
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-chloro-N'-hydroxyethanimidamide | HCID 4112252 | — |
| Product | 3-Chloromethyl-5-cyanomethyl-1,2,4-oxadiazole | HCID 20161213 | 55.8% |
Reaction Steps
To a solution of 8.50 g of cyanoacetic acid and 10.1 g of chloroacetamidoxime was added 20.6 g of N,N'-dicyclohexylcarbodiimide with ice-cooling. After stirring for 1 hour at room temperature, the reaction mixture was filtered and the filtrate was concentrated in vacuo. The residue was triturated with 20 ml of ethyl acetate and the insoluble material was filtered off and washed with ethyl acetate. The filtrate was then concentrated in vacuo and the residue was dissolved in 50 ml of toluene. The resultant solution was heated under reflux for 20 minutes with a water separator. After cooling and adding 50 ml of ethyl acetate, the solution was decanted and evaporated in vacuo. The residue was chromatographed on silica gel using chloroform-methanol (50:1) as eluent to give 8.18 g of 3-chloromethyl-5-cyanomethyl-1,2,4-oxadiazole as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04705786 |
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| Source dataset | uspto-grants-1987_11 |
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| ORD ID | ord-6da515c00d124e6cbaab78c80c261cf8 |
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| Source note | uspto-grants-1987_11 |
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