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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78279생성일: 2026년 10월 25일

Acetic Acid → 1-Benzyloxy-4-(2-nitro-ethyl)-benzene

https://huagongshe.com/reaction/78279

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Dimethyl SulfoxideHCID 679—
반응물(E)-1-(Benzyloxy)-4-(2-nitrovinyl)benzeneHCID 5702926—
반응물VertellusHCID 22959485—
용매WaterHCID 962—
생성물1-Benzyloxy-4-(2-nitro-ethyl)-benzeneHCID 24721037—

반응 단계

While cooling using a water bath, to a mixture of 1-benzyloxy-4-((E)-2-nitro-vinyl)-benzene described in Manufacturing Example 229-1-1 (60 g, 0.23 mol), acetic acid (27 mL) and dimethyl sulfoxide (400 mL) was added sodium borohydrate (8.9 g, 0.23 mol), which was stirred for 20 minutes at room temperature. Water (2.5 L) was added dropwise to the reaction mixture, and the deposited solids were filtered. Diethyl ether (300 mL) was added to the obtained solids to dissolve the title compound, and separation into filtrate and solids was carried out by filtration. The filtrate was concentrated under a reduced pressure to obtain the title compound (39 g). On the other hand, diethyl ether (300 mL) was added to the previously separated solid to dissolve the title compound, and separation into filtrate and solids was carried out by filtration. The filtrate was concentrated under a reduced pressure to obtain the title compound (12 g). This was combined with the previously obtained solids to obtain the title compound (51 g) as a crude product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841327B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-a3349ff6394d4fd3981d78e8162ad706
출처 메모uspto-grants-2014_09