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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359239Generated: October 30, 2026

Ethyl vinyl ether → HCID 58432122, compound

https://huagongshe.com/reaction/2359239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl vinyl etherHCID 8023—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Hydroxy-3-methoxy-3-(4-morpholinophenyl)propanenitrileHCID 58432084—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 58432122HCID 5843212235.5%

Reaction Steps

To a solution of 2-hydroxy-3-methoxy-3-(4-morpholinophenyl)propanenitrile (˜5.1 mmol) in anhydr CH2Cl2 (17 mL) under argon was added pyridinium para-toluenesulfonate (0.094 g, 0.37 mmol) and ethyl vinyl ether (17 mL, 178 mmol). The mixture was placed under a drying tube and stirred at room temperature for 16 hrs. Additional ethylvinyl ether (4 mL, 42 mmol) and pyridinium para-toluenesulfonate (0.11 g, 0.44 mmol) were added and the mixture stirred for 24 hrs more. Saturated aqueous NaHCO3 was added to the mixture then it was diluted with H2O and CH2Cl2. The layers were separated and the aqueous layer was extracted with CH2Cl2. The combined organics were washed with brine, dried over MgSO4 and concentrated in vacuo. Purification by chromatography (20-35% EtOAc-hexanes containing 1% Et3N) gave 2-(1-ethoxyethoxy)-3-methoxy-3-(4-morpholinophenyl)propanenitrile (0.606 g, 35% for three steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685975B2
Source datasetuspto-grants-2014_04
ORD IDord-58dcb29952384dec8df061685e640532
Source noteuspto-grants-2014_04