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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17699생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/17699

반응식

참여 물질

역할이름HCID투입량
반응물4'-HydroxyacetophenoneHCID 7469—
반응물Potassium CarbonateHCID 11430—
반응물3-(Diethylamino)-1-propanolHCID 12159—
반응물Methanesulfonyl chlorideHCID 31297—
반응물MethanesulfonateHCID 85257—
용매DimethylformamideHCID 6228—
생성물1-(4-[3-(Diethylamino)propoxy]phenyl)ethanoneHCID 11858361—

반응 조건

온도80 °C

반응 단계

To a stirred solution of 4′-hydroxyacetophenone (91 mmol) in DMF (80 mL) at rt, solid potassium carbonate (153 mmol) was added. The mesylate prepared from 3-diethylamino-1-propanol and methanesulfonyl chloride (76 mmol) was added to the reaction mixture and heated to 80° C. until completion according to General Procedure Q1, as indicated by TLC or HPLC. After cooling to rt, the reaction mixture was quenched by treating the mixture with saturated sodium bicarbonate. The aqueous layer was poured into EtOAc (100 mL) and washed with H2O (2×50 mL) and brine (50 mL). The organic layer was dried over sodium sulfate, and the solvent was removed in vacuuo to afford the desired 1-{4-[3-(diethylamino)propoxy]phenyl}ethanone. The crude alkylated product was used for further transformation after purifying using silica gel column chromatography (1-4% MeOH/DCM).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737285B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-30834c4dd61b49dc904e22cfb6d1f1b8
출처 메모uspto-grants-2010_06