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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154791Generated: October 31, 2026

Hydrochloric Acid → 2-Methoxyimino-3,3-ethylenedioxybutyric acid

https://huagongshe.com/reaction/1154791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-methoxyimino-3,3-ethylenedioxybutyrateHCID 54382027—
SolventEthanolHCID 702—
Product2-Methoxyimino-3,3-ethylenedioxybutyric acidHCID 5445240599.3%

Reaction Steps

To a solution of ethyl 2-methoxyimino-3,3-ethylenedioxybutyrate (syn isomer, 180 g) in ethanol (1080 ml) was added 1 N aqueous solution of sodium hydroxide (1660 ml) and the mixture was stirred for 2 hours and 10 minutes at ambient temperature. After the reaction mixture was adjusted to pH 7.3 with 6 N hydrochloric acid, ethanol was distilled off under reduced pressure and then washed with diethyl ether (500 ml×2). To the resultant was added diethyl ether (1 l), adjusted to pH 1.5 with 6 N hydrochloric acid and then diethyl ether layer was separated. The remaining aqueous layer was further extracted with diethyl ether (350 ml), and the remaining aqueous layer was adjusted to pH 1.3 with 6 N hydrochloric acid and then further extracted with diethyl ether (350 ml×2). The diethyl ether layer and extracts were combined together, washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and then filtered. The filtrate was concentrated to give an oil (155.6 g) of 2-methoxyimino-3,3-ethylenedioxybutyric acid (syn isomer). (Yield: 99.3%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04298529
Source datasetuspto-grants-1981_11
ORD IDord-3fb84a62917c406e9ae922bd534f70f4
Source noteuspto-grants-1981_11