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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67796생성일: 2026년 10월 24일

2-Phenylethanol → 1-Nitro-3-(2-phenylethoxy)benzene

https://huagongshe.com/ko/reaction/67796

반응식

참여 물질

역할이름HCID투입량
반응물2-PhenylethanolHCID 6054—
반응물1,3-DinitrobenzeneHCID 7452—
반응물HexamethylphosphoramideHCID 12679—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
생성물1-Nitro-3-(2-phenylethoxy)benzeneHCID 13052313219.9%

반응 단계

Potassium t-butoxide (11.2 g; 0.1 mol) is added under a nitrogen atmosphere to a stirred mixture of m-dinitrobenzene (16.8 g; 0.1 mol), phenethyl alcohol (12.2 g; 0.1 mol) and hexamethylphosphoramide (HMPA; 200 ml). Almost instantly a dark red color develops and then slowly fades in the course of the reaction and turns black. The reaction mixture is stirred for 7 days at room temperature. It is then drowned in water, and extracted twice with methylene chloride (500 ml). The methylene chloride solution is washed with water (3X), saturated brine (1X), dried over magnesium sulfate and evaporated to yield 53.5 g of a dark oil. Additional solvent (HMPA) and some m-dinitrobenzene is removed from the oil by heating same at about 90° C. under 0.5 mm vacuum. The residual oil (~25 g) is chromatographed on 1 kg silica gel with 3:1 hexane:methylene chloride. Collected fractions, containing the same material by thin layer chromatography, are combined and evaporated to afford 7.4 g (30%) of product, a light yellow oil. On standing, the oil crystallizes, mp. 46.5°-49° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04346242
출처 데이터셋uspto-grants-1982_08
ORD IDord-98a6af63fb1049dc8ef9e98988a49156
출처 메모uspto-grants-1982_08