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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 262012생성일: 2026년 10월 24일

2-Nitrophenol → 1-(Cyclopentyloxy)-2-nitrobenzene

https://huagongshe.com/ko/reaction/262012

반응식

참여 물질

역할이름HCID투입량
반응물2-NitrophenolHCID 6947—
반응물BromocyclopentaneHCID 8728—
반응물Potassium CarbonateHCID 11430—
용매AcetoneHCID 180—
생성물1-(Cyclopentyloxy)-2-nitrobenzeneHCID 2216447346.8%

반응 단계

2-Nitrophenol (83.5 g, 0.60 mole), cyclopentyl bromide (98.0 g, 0.66 mole), anhydrous potassium carbonate (82.9 g, 0.60 mole) and dry acetone (600 cc) were refluxed for 72 hrs., and filtered to remove the potassium bromide. The residue was washed with acetone and the solvent was removed by rotary evaporation. The residue was partitioned between 200 cc of dichloromethane and water. The dichloromethane layer was washed with 200 cc of 10% potassium hydroxide, separated and the solvent was removed by rotary evaporation. The crude product was fractionally distilled at 144°-146° C. at 1.0 mm. Hg to yield 58.2 g of product (46.8%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04153446
출처 데이터셋uspto-grants-1979_05
ORD IDord-9cc3f965c1b640e1b7d43fc85411ead5
출처 메모uspto-grants-1979_05