HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463391Generated: October 26, 2026
Ethylene Glycol → Ethyl 2-hydroxyimino-3,3-ethylenedioxy-4-chlorobutyrate
https://huagongshe.com/reaction/463391
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | HCID 178472915 | HCID 178472915 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl 2-hydroxyimino-3,3-ethylenedioxy-4-chlorobutyrate | HCID 86738087 | 58.9% |
Reaction Steps
A mixture of ethyl 2-hydroxyimino-3-oxo-4-chlorobutyrate (syn isomer, 10 g), ethylene glycol (16 g), p-toluenesulfonic acid (0.3 g) and dried benzene (100 ml) was heated for 19 hours under reflux while removing water azeotropically. After the reaction mixture was cooled to ambient temperature, water (30 ml) and benzene (20 ml) were added thereto. The mixture was saturated with sodium chloride and the benzene layer was separated, and the remaining aqueous layer was further extracted with benzene (20 ml). The benzene layer and extract were combined together, washed with a saturated aqueous solution of sodium chloride (30 ml×2), dried over magnesium sulfate and then filtered. The filtrate was evaporated to give an oil of ethyl 2-hydroxyimino-3,3-ethylenedioxy-4-chlorobutyrate (syn isomer, 7.23 g). (Yield: 58.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04518774 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-53e97e69cd444e98a831d80385a1df68 |
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| Source note | uspto-grants-1985_05 |
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