HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426890Generated: October 31, 2026
Ethylene Glycol → Benzyl oximino-acetoacetate ethylene ketal
https://huagongshe.com/reaction/426890
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 86734531 | HCID 86734531 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Benzyl oximino-acetoacetate ethylene ketal | HCID 86734545 | 94% |
Reaction Steps
In a two liter flask fitted with a Dean Stark water separator and a condenser were placed in 186.5 g. (0.85 mole) of benzyl oximino-acetoacetate [1.1], 62 g. (1 mole) of ethylene glycol, 800 ml. of benzene (reagent grade) and 2 g. (10.5 mmole) of p-toluenesulfonic acid monohydrate. The reaction mixture was boiled at reflux until 15 ml. of water was removed (3 hours). The benzene solution was washed once with saturated sodium bicarbonate solution and once with brine. After drying over anhydrous sodium sulfate, the benzene solution was evaporated, leaving 212 g. (94% yield) of benzyl oximino-acetoacetate ethylene ketal [2.1] as a light yellow oil! Its NMR spectrum was consistent with the assigned structure. Generally, the product was used as such in subsequent reactions but one of the isomers can be crystallized2 from toluene-petroleum either (b.p. 30°-60° C.); m.p. 52° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04171438 |
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| Source dataset | uspto-grants-1979_10 |
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| ORD ID | ord-fc1ea6eaeda34dd2b4bf2b73d7ec0e38 |
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| Source note | uspto-grants-1979_10 |
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