HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22294Generated: October 29, 2026
Ethyl orthoformate → HCID 9837432, compound
https://huagongshe.com/reaction/22294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | HCID 53776389 | HCID 53776389 | — |
| Catalyst | Boron trifluoride etherate | HCID 8000 | — |
| Product | HCID 9837432 | HCID 9837432 | 57.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05428047 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-37b961b7618c4f79bcf7539528f74aad |
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| Source note | uspto-grants-1995_06 |
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