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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4726생성일: 2026년 10월 24일

4'-Hydroxyacetophenone → 1-[4-(3-Chloropropoxy)phenyl]ethanone

https://huagongshe.com/ko/reaction/4726

반응식

참여 물질

역할이름HCID투입량
반응물4'-HydroxyacetophenoneHCID 7469—
반응물1-Bromo-3-chloropropaneHCID 8006—
반응물Potassium HydroxideHCID 14797—
용매MethanolHCID 887—
생성물1-[4-(3-Chloropropoxy)phenyl]ethanoneHCID 1268561368%

반응 단계

To a mixture of p-hydroxyacetophenone (50.7 g, 0.37 mol) and 1-bromo-3-chloropropane (160 ml, 1.5 mol) in methanol (250 ml) was added portionwise potassium hydroxide (63 g, 1.12 mol). The mixture was stirred at reflux for 24 hours, cooled to room temperature, filtered through Celite and evaporated in vacuo. The residual semi-solid was diluted with diethyl ether (500 ml) and washed with H2O (2×300 ml). The ether solution was dried over MgSO4, filtered and evaporated in vacuo to give p-chloropropoxy acetophenone as a liquid in 68% yield (53.38 g). 1H NMR (CDCl3): δ7.98-7.89 (d, J=8.9 Hz, 2H), 7.02-6.92 (d, J=8.9 Hz, 2H), 4.16 (t, J=5.9 Hz, 2H), 3.75 (t, J=6.4 Hz, 2H), 2.52 (s, 3H), 2.34-2.16 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727145
출처 데이터셋uspto-grants-1988_02
ORD IDord-79c238d7b16349c6ba9878c87b186e20
출처 메모uspto-grants-1988_02