HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → Ethyl 2-methoxyimino-3,3-ethylenedioxybutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl (2Z)-2-methoxyimino-3-oxo-butanoate | HCID 43493 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | Ethyl 2-methoxyimino-3,3-ethylenedioxybutyrate | HCID 54382027 | 85.5% |
Reaction Steps
To a solution of ethyl 2-methoxyimino-3-oxobutyrate (syn isomer, 200 g) in ethylene glycol (179 g) were added dried benzene (3 l) and p-toluenesulfonic acid (6 g), and the mixture was heated for 20 hours under reflux while removing water azeotropically. The reaction mixture was cooled to ambient temperature, washed with water, a saturated aqueous solution of sodium bicarbonade, water and a saturated aqueous solution of sodium chloride in turn, dried over magnesium sulfate and then filtered. After the filtrate was evaporated, the residual oil was distilled under reduced pressure to give ethyl 2-methoxyimino-3,3-ethylenedioxybutyrate (syn isomer), bp 89.5°-91° C./0.6 mmHg, in 85.5% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04518774 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-26fba6fe5ea54788b9e49e89718a4798 |
| Source note | uspto-grants-1985_05 |