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HRID 5951作成日:2026年10月26日

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

https://huagongshe.com/reaction/5951

反応式

関与物質

役割名称HCID仕込み量
反応物O-Methylhydroxylamine hydrochlorideHCID 521874—
反応物[2R,3R]-2,3-Bis(((1,1-dimethylethyl)dimethylsilyl)oxymethyl)cyclobutanoneHCID 54324527—
溶媒PyridineHCID 1049—
生成物[2R,3R]-2,3-Bis(((1,1-dimethylethyl)di-methylsilyl)oxymethyl)cyclobutanone-O-methyl oximeHCID 8674723475.7%

反応手順

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)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05246931
出典データセットuspto-grants-1993_09
ORD IDord-d480d233dea742e5bf153c3b7f49c34c
出典メモuspto-grants-1993_09