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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154803Generated: November 3, 2026

Methanol → HCID 54165460, compound

https://huagongshe.com/reaction/1154803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl (2Z)-2-methoxyimino-3-oxo-butanoateHCID 43493—
ReactantMethylorthoformateHCID 53629101—
ProductHCID 54165460HCID 54165460—

Reaction Steps

Methyl orthoformate (31.8 g) and "Amberlist 15" (trademark) (1.7 g) were added to a stirred solution of ethyl 2-methoxyimino-3-oxobutyrate (syn isomer, 17.3 g) in dry methanol (50 ml) and stirred at 50° to 60° C. for 2.5 hours. To the resultant solution was added methyl orthoformate (10.6 g) and stirred for 2 hours. The solution was allowed to stand in refrigerator overnight and stirred at 50° to 60° C. for 2 hours. After evaporating methanol in vacuo, diethyl ether (100 ml) and water (50 ml) were added to the residue, and the organic layer was separated. The aqueous layer was extracted with diethyl ether. The organic layer and the extract were combined together and washed with a saturated aqueous solution of sodium chloride. The solution was dried over magnesium sulfate and evaporated under reduced pressure to give ethyl 2-methoxyimino-3,3-dimethoxybutyrate (syn isomer, 18 g). bp 61° to 64° C./0.35 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04298529
Source datasetuspto-grants-1981_11
ORD IDord-5687e4bc466149b187c40d1a251f32bd
Source noteuspto-grants-1981_11