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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 640235생성일: 2026년 10월 24일

Acetic Acid → 1-Benzyloxy-3-(2-nitro-ethyl)-benzene

https://huagongshe.com/ko/reaction/640235

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium borohydrideHCID 4311764—
반응물3-Benzyloxy-trans-beta-nitrostyreneHCID 5368282—
용매Dimethyl SulfoxideHCID 679—
생성물1-Benzyloxy-3-(2-nitro-ethyl)-benzeneHCID 5925520557%

반응 단계

To an acetic acid (5.5 mL) and dimethyl sulfoxide (94 mL) solution of 1-benzyloxy-3-((E)-2-nitro-vinyl)-benzene (5.5 g, 21.5 mmol) described in Manufacturing Example 61-1-2 was added sodium borohydride (1.3 g, 34.4 mmol) at room temperature while cooling appropriately. This mixture was stirred for 1.5 hours at room temperature. This mixture was partitioned into ethyl acetate and water. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by silica gel column chromatography (heptane:ethyl acetate=10:1-4:1) to obtain the title compound (3.14 g, 57%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07691882B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-f3312406b5254db9a4b4b5865306b900
출처 메모uspto-grants-2010_04