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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 217986Erstellt: 24. Oktober 2026

Ethanol → ((R)-1-benzyloxymethyl-3-butenyloxy)acetaldehyde oxime

https://huagongshe.com/de/reaction/217986

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktHydroxylamine, sulfate (1:1)HCID 159255—
EduktSodium AcetateHCID 517045—
Edukt[(R)-2-(2,2-diethoxyethoxy)-4-pentenyloxymethyl]benzeneHCID 59281174—
LösungsmittelFormic AcidHCID 284—
LösungsmittelWaterHCID 962—
Produkt((R)-1-benzyloxymethyl-3-butenyloxy)acetaldehyde oximeHCID 86640913112,9%

Reaktionsschritte

[(R)-2-(2,2-Diethoxyethoxy)-4-pentenyloxymethyl]benzene (20.0 g) was dissolved in formic acid (160 ml) and water (40 ml), and the mixture was stirred at room temperature for 30 minutes. Next, water (161 ml) and ethanol (400 ml) were added, and then hydroxylamine sulfate (6.38 g) and sodium acetate (8.82 g) were added, followed by stirring at room temperature overnight. Water was added to the reaction solution, and the insoluble matter was dissolved. Then, the excess of ethanol was evaporated under reduced pressure. The aqueous layer was extracted with ethyl acetate. The organic layer was washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound (13.7 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08198269B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-8153b949c99546c7bd78cf01a586fb24
Quellennotizuspto-grants-2012_06