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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702033Generated: October 30, 2026

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

https://huagongshe.com/reaction/1702033

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 numberUS04379922
Source datasetuspto-grants-1983_04
ORD IDord-5d83cc89191d466ab03998a6e5763834
Source noteuspto-grants-1983_04