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HRID 5951Erstellt: 23. Oktober 2026

O-Methylhydroxylamine hydrochloride → [2R,3R]-2,3-Bis(((1,1-dimethylethyl)di-methylsilyl)oxymethyl)cyclobutanone-O-methyl oxime

https://huagongshe.com/de/reaction/5951

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktO-Methylhydroxylamine hydrochlorideHCID 521874—
Edukt[2R,3R]-2,3-Bis(((1,1-dimethylethyl)dimethylsilyl)oxymethyl)cyclobutanoneHCID 54324527—
LösungsmittelPyridineHCID 1049—
Produkt[2R,3R]-2,3-Bis(((1,1-dimethylethyl)di-methylsilyl)oxymethyl)cyclobutanone-O-methyl oximeHCID 8674723475,7%

Reaktionsschritte

A solution of 12.317 g (34.9 mmol) of [2R,3R]-2,3-Bis(((1,1-dimethylethyl)dimethylsilyl)oxymethyl)cyclobutanone, from Step E, in 20 mL of pyridine was added to a solution of 3.160 g (37.8 mmol) of methoxylamine hydrochloride in 80 mL of pyridine. After stirring the reaction mixture for 70 min at ambient temperature, it was concentrated to approximately 1/4 of the original volume then diluted with ethyl acetate, washed with saturated aqueous sodium bicarbonate solution, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography on a 5×38 cm silica gel column eluted with 1 L of hexane and 5% acetone in hexane to give 10.228 g (75.7% yield) of the title compound as a mixture of geometrical isomers. .MS DCI-NH3M/Z: 388 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05246931
Quelldatensatzuspto-grants-1993_09
ORD IDord-d480d233dea742e5bf153c3b7f49c34c
Quellennotizuspto-grants-1993_09