HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462043Generated: November 2, 2026
Water → (Z)-2-Methoxyimino-3-oxobutyric acid, 1,1-dimethylethyl ester
https://huagongshe.com/reaction/1462043
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178468383 | HCID 178468383 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (Z)-2-Methoxyimino-3-oxobutyric acid, 1,1-dimethylethyl ester | HCID 6420338 | — |
Reaction Steps
626.65 g of (Z)-2-hydroxyimino-3-oxo-butyric acid tert.butyl ester are dissolved in 2.86 l of acetone. The solution is cooled to 5° C. and treated portionwise with 703.5 g of potassium carbonate. 322 ml of dimethyl sulphate are then added dropwise to the yellow suspension without cooling during 1 hour, whereby the temperature of the mixture should not rise above 25° C. The light beige suspension is stirred at 20°-25° C. for about 4 hours until starting material can no longer be detected by thin-layer chromatography. Thereafter, the mixture is poured into 7 l of water and extracted three times with 1 l of ethyl acetate each time. The combined ethyl acetate extracts are washed three times with 1 l of water each time, dried over sodium sulphate and evaporated in vacuo at 40° C. The residual yellow oil is dried for a further 6 hours in a high vacuum at 40° C. and subsequently distilled. There is obtained (Z)-2methoxyimino-3-oxo-butyric acid tert.butyl ester as a yellow oil with a boiling point of 57° C. at 0.02 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04458072 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-d0c486bce5fd4337b5ddd244155cded6 |
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| Source note | uspto-grants-1984_07 |
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