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HRID 1087002作成日:2026年10月26日

Triphenyl phosphite → 4-[2-[4-(t-Butyl)phenyl]ethoxy]pteridine

https://huagongshe.com/reaction/1087002

反応式

関与物質

役割名称HCID仕込み量
反応物Triphenyl phosphiteHCID 7540—
反応物ChlorineHCID 24526—
反応物p-tert-Butylphenethyl alcoholHCID 79410—
反応物HCID 178518044HCID 178518044—
溶媒PyridineHCID 1049—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
生成物4-[2-[4-(t-Butyl)phenyl]ethoxy]pteridineHCID 14996113—

反応条件

温度-17.5 °C

反応手順

To a suspension of 2 g of 4-hydroxypteridine in 20 mL of CH2Cl2 under nitrogen was added 1.2 g of 25 pyridine. The mixture was cooled to -30° C and over a 15 minute period a solution of 4.82 g of triphenyl phosphite in CH2Cl2 was added simultaneously with addition of chlorine gas. The mixture was stirred for one and one half hours while maintaining the temperature at -15 to -20° C. The mixture was then allowed to warm to 10° C., and a solution of 2.67 g of 2-[4-(t-butyl)phenyl]ethanol in CH2Cl2 was added. The resulting mixture was refluxed for 45 minutes, then cooled and diluted into toluene. The toluene solution was washed with dilute base, then filtered through phase separating paper and concentrated in vacuo. The resulting bluish oil was adsorbed onto silica gel and chromatographed (silica gel, CH2Cl2 →80% CH2Cl2, 20% EtOAc). Fractions containing the major product were combined. The product was then recrystallized from petroleum ether/CH2Cl2. Yield 60 mg. M.P. 149° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05034393
出典データセットuspto-grants-1991_07
ORD IDord-c7b84f61f4e3445b8876ade0e5030088
出典メモuspto-grants-1991_07