戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 217986作成日:2026年10月26日

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

https://huagongshe.com/reaction/217986

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Hydroxylamine, sulfate (1:1)HCID 159255—
反応物Sodium AcetateHCID 517045—
反応物[(R)-2-(2,2-diethoxyethoxy)-4-pentenyloxymethyl]benzeneHCID 59281174—
溶媒Formic AcidHCID 284—
溶媒WaterHCID 962—
生成物((R)-1-benzyloxymethyl-3-butenyloxy)acetaldehyde oximeHCID 86640913112.9%

反応手順

[(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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198269B2
出典データセットuspto-grants-2012_06
ORD IDord-8153b949c99546c7bd78cf01a586fb24
出典メモuspto-grants-2012_06