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HRID 353300作成日:2026年10月26日

Potassium Carbonate → Ethyl 3-[3-tert-butyl-4-(2-{4-[(methylsulfonyl)oxy]phenyl}ethoxy)phenyl]-2-ethoxypropanoate

https://huagongshe.com/reaction/353300

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1-(Methylsulfonyloxy)-2-[4-(methylsulfonyloxy)phenyl]ethaneHCID 11220122—
反応物Ethyl 3-(3-tert-butyl-4-hydroxyphenyl)-2-ethoxypropanoateHCID 22708416—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物Ethyl 3-[3-tert-butyl-4-(2-{4-[(methylsulfonyl)oxy]phenyl}ethoxy)phenyl]-2-ethoxypropanoateHCID 1030019522.1%

反応手順

Ethyl 3-(3-tert-butyl-4-hydroxyphenyl)-2-ethoxypropanoate (0.15 g, 0.44 mmole) and 4-{2-[(methylsulfonyl)oxy]ethyl}phenyl methanesulfonate (0.26 g, 0.89 mmole) were dissolved in 2-butanone (4 ml). Polyethyleneglycol 400 (0.05 g) and anhydrous potassium carbonate (0.092 g, 0.67 mmole) were added the mixture. After stirring at reflux for 16 hours it was checked using HPLC whether all the starting material was consumed. The mixture was washed with water dried with magnesium sulfate and evaporated. Purification of the crude product with preparative HPLC (Kromasil C8, 7 μm, 50×250 mm) using actonitrile(40-80%) in ammonium acetate buffer (pH 7) as mobile phase gave 0.048 g (22% yield) of the desired product

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06750252B2
出典データセットuspto-grants-2004_06
ORD IDord-4cada9979f354ec8bfeed55abff49f4d
出典メモuspto-grants-2004_06