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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217986생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/217986

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Hydroxylamine, sulfate (1:1)HCID 159255—
반응물Sodium AcetateHCID 517045—
반응물[(R)-2-(2,2-diethoxyethoxy)-4-pentenyloxymethyl]benzeneHCID 59281174—
용매Formic AcidHCID 284—
용매WaterHCID 962—
생성물((R)-1-benzyloxymethyl-3-butenyloxy)acetaldehyde oximeHCID 86640913112.9%

반응 단계

[(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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198269B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-8153b949c99546c7bd78cf01a586fb24
출처 메모uspto-grants-2012_06