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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22294Generated: October 29, 2026

Ethyl orthoformate → HCID 9837432, compound

https://huagongshe.com/reaction/22294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantHCID 53776389HCID 53776389—
CatalystBoron trifluoride etherateHCID 8000—
ProductHCID 9837432HCID 983743257.4%

Reaction Steps

7.0 g (32.6 mmol) of 3-chloro-2-methyl-phenoxy-acetamide oxime are introduced into 70 ml of triethyl orthoformate, and 5 drops of boron trifluoride etherate are added at room temperature. The mixture is subsequently stirred at reflux temperature until the reaction is complete (approximately 1 hour) and the entire batch is concentrated in vacuo. The residue is taken up in 100 ml of methylene chloride and washed in succession with 100 ml of 2N hydrochloric acid, saturated sodium carbonate solution and water. The organic phase is dried over sodium sulphate and the solvent is subsequently distilled off. The oily residue which remains is distilled using a bulb tube. 4.2 g (57.4% of theory) of 3-(3-chloro-2-methyl-phenoxymethyl)-1,2,4-oxadiazole are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428047
Source datasetuspto-grants-1995_06
ORD IDord-37b961b7618c4f79bcf7539528f74aad
Source noteuspto-grants-1995_06