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HRID 17697作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/17697

反応式

関与物質

役割名称HCID仕込み量
反応物4'-HydroxyacetophenoneHCID 7469—
反応物Potassium CarbonateHCID 11430—
反応物3-(Diethylamino)-1-propanolHCID 12159—
反応物Methanesulfonyl chlorideHCID 31297—
反応物MethanesulfonateHCID 85257—
溶媒DimethylformamideHCID 6228—
生成物1-(4-[3-(Diethylamino)propoxy]phenyl)ethanoneHCID 11858361—

反応条件

温度80 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737285B2
出典データセットuspto-grants-2010_06
ORD IDord-8310e01060ad4b869e476204a2d27343
出典メモuspto-grants-2010_06