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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765455Generated: October 25, 2026

Hydrochloric Acid → 3,3-Dimethoxy-2-hydroxyiminopropionitrile

https://huagongshe.com/reaction/1765455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantNitrosyl chlorideHCID 17601—
Reactant3-Methoxy-2-propenenitrileHCID 2723755—
ReactantSodium NitriteHCID 23668193—
Product3,3-Dimethoxy-2-hydroxyiminopropionitrileHCID 7136156280.1%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a flask having an inner volume of 300 ml and equipped with a stirring device, a thermometer, a condenser and a gas inlet tube were charged 42.83 g (0.5 mol) of 3-methoxyacrylonitrile with a purity of 97% by weight and 125 ml of methanol, and the mixture was cooled to −10° C. under stirring. Then, the reaction solution was maintained to −10 to 0° C., and while feeding nitrosyl chloride generated by reacting 170.5 g (1.0 mol) of 41% by weight aqueous sodium nitrite solution and 320 ml (3.5 mol) of conc. hydrochloric acid (the above-mentioned method (2)) in a separate apparatus to the reaction solution, the resulting mixture was reacted at −10 to 0° C. for 3 hours and at room temperature for 2 hours. After completion of the reaction, the reaction mixture was concentrated under reduced pressure, the concentrate was washed in the order of n-hexane and toluene, dried under reduced pressure at 40° C. to obtain 61.6 g of 3,3-dimethoxy-2-hydroxyiminopropionitrile (Isolation yield: 80.1%) as a pale yellowish solid with a purity of 93.7% by weight (absolute calibration curve method by high performance liquid chromatography).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07227032B2
Source datasetuspto-grants-2007_06
ORD IDord-0ce93b153faf48c2a1d313fee03254da
Source noteuspto-grants-2007_06