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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031230Generated: October 29, 2026

Water → Tert-butyl 2-methoxyimino-3-oxobutyrate

https://huagongshe.com/reaction/1031230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethyl SulfateHCID 6497—
ReactantSodium HydroxideHCID 14798—
Reactanttert-butyl 2-hydroxyimino-3-oxobutanoateHCID 178468384—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 2-methoxyimino-3-oxobutyrateHCID 5411035293.3%

Reaction Steps

To the tert-butyl 2-hydroxyimino-3-oxobutyrate was added water [6], to which was added 30% sodium hydroxide [800 ml] at 28° C. while stirring to render the pH to 9.0. To the resultant solution was added dimethyl sulfate [1324 g] at 28° to 30° C. in the course of 20 minutes, which was stirred for 4 hours while adding thereto at 25° to 30° C. a 30% aqueous solution of sodium hydroxide [500 ml] to adjust the pH within the range of 8.7 to 9.0. After completion of the reaction, extraction was conducted with methylene chloride [4 l], and the aqueous layer was subjected to further extraction with methylene chloride [2 l]. The methylene chloride layers were combined and washed with a 1N aqueous solution of sodium hydroxide, 1N HCl, a 5% aqueous solution of sodium hydrogencarbonate and water, each one litre portion, successively. The resultant solution was dried over anhydrous sodium sulfate [700 g], followed by concentration under reduced pressure to obtain tert-butyl 2-methoxyimino-3-oxobutyrate [1878 g] as an oily product. The yield was 93.3%. NMR(CDCl3): δ4.08 (3H,s), 2.36(3H,s), 1.53(9H,s)ppm .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05109131
Source datasetuspto-grants-1992_04
ORD IDord-fde0c3ccd0ed4f1aa21f8d9ed04483fc
Source noteuspto-grants-1992_04