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HRID 2264281作成日:2026年10月26日

Ammonium Chloride → 8-(2,4,5-Trifluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol

https://huagongshe.com/reaction/2264281

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物1-Bromo-2,4,5-trifluorobenzeneHCID 67597—
反応物1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物8-(2,4,5-Trifluorophenyl)-1,4-dioxaspiro[4.5]decan-8-olHCID 57424359—

反応条件

温度50 °C

反応手順

A three neck flask (2 L) under an atmosphere of nitrogen with Mg turnings (9.8 g) was stirred for 15 min and tetrahydrofuran (90 mL) was added and stirring continued for an additional 15 min. 1-Bromo-2,4,5-trifluorobenzene (85 g) was dissolved in tetrahydrofuran (340 mL). A portion of this solution (75 mL) was added to the stirred magnesium turnings and then heated to 50° C. The rest of the solution was added and stirring continued at the same temperature for an additional 1 h. The reaction mixture was cooled to 40° C., a solution of 1,4-dioxaspiro[4.5]decan-8-one (57.3 g) in tetrahydrofuran (275 mL) was added, and stirring continued for 10 h. The reaction mixture was poured into saturated aqueous ammonium chloride solution (970 mL) and extracted with toluene (700 mL). The organic layer was washed with water (3×700 mL), dried over anhydrous sodium sulfate, filtered and evaporated to yield the title compound as a red-orange oil which was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07855206B2
出典データセットuspto-grants-2010_12
ORD IDord-22cfae6d14044f4081edddd14ab9699a
出典メモuspto-grants-2010_12