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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733726Generated: November 1, 2026

Sodium Hydroxide → 2-(2,3-Dihydro-1,4-oxathiin-6-yl)-2-n-propoxyiminoacetic acid

https://huagongshe.com/reaction/1733726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(2,3-dihydro-1,4-oxathiin-6-yl)-2-n-propoxyiminoacetateHCID 54220578—
SolventMethanolHCID 887—
Product2-(2,3-Dihydro-1,4-oxathiin-6-yl)-2-n-propoxyiminoacetic acidHCID 5378366033.6%

Reaction Steps

Ethyl 2-(2,3-dihydro-1,4-oxathiin-6-yl)-2-n-propoxyiminoacetate (mixture of syn isomer and anti isomer, 1 g.) was added to a mixture of methanol (10 ml.) and 1 N aqueous solution of sodium hydroxide (6 ml.), and stirred at room temperature for 18 hours. After distilling off the methanol from the resultant solution in vacuo, a saturated aqueous solution of sodium bicarbonate (15 ml.) and ethyl acetate (15 ml.) were added to the residue and shaken sufficiently. The aqueous layer was separated, adjusted to pH 1.0 with 10% hydrochloric acid and extracted with ethyl acetate (20 ml.). The extract was washed with water, dried over magnesium sulfate and concentrated in vacuo. The residue was triturated with a mixture of n-hexane and diethyl ether (1:1). The precipitates were collected by filtration and washed with the same mixture to give 2-(2,3-dihydro-1,4-oxathiin-6-yl)-2-n-propoxyiminoacetic acid (syn isomer, 0.30 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242510
Source datasetuspto-grants-1980_12
ORD IDord-cd6bd4328de94690aa74c7181e5c2c64
Source noteuspto-grants-1980_12