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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982016Generated: October 28, 2026

Sulfuric Acid → 2-Methoxyimino-3,3-ethylenedioxy-4-bromobutyric acid

https://huagongshe.com/reaction/1982016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-methoxyimino-3,3-ethylenedioxy-4-bromobutyrateHCID 53760491—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-Methoxyimino-3,3-ethylenedioxy-4-bromobutyric acidHCID 5367572774.8%

Reaction Steps

A solution of sodium hydroxide (8.64 g) in water (20 ml) was added to a solution of ethyl 2-methoxyimino-3,3-ethylenedioxy-4-bromobutyrate (syn isomer, 26.6 g) in methanol (60 ml) under ice-cooling, stirred at ambient temperature for 2 hours. Water (100 ml) was added to the resultant solution and adjusted to pH 7.0 with 20% sulfuric acid under ice-cooling. After removing methanol therefrom in vacuo, the solution was washed with diethyl ether (100 ml). Diethyl ether (100 ml) was added to the aqueous layer and adjusted to pH 2.0 with 20% sulfuric acid below 10° C. The organic layer was separated, and then the aqueous layer was extracted with diethyl ether (100 ml) twice. The organic layer was washed with water and a sodium chloride saturated aqueous solution in turn, and dried over magnesium sulfate. The solution was concentrated in vacuo and the residue was allowed to stand in refrigerator overnight to give 2-methoxyimino-3,3-ethylenedioxy-4-bromobutyric acid (syn isomer, 18.0 g.). (Yield: 74.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04594446
Source datasetuspto-grants-1986_06
ORD IDord-26163d9e55da4c9990ae73b176781baf
Source noteuspto-grants-1986_06