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HRID 2371728作成日:2026年10月27日

Phosgene → 3-(2-Chloro-4-fluorophenoxy)-1-azetidinecarbonyl chloride

https://huagongshe.com/reaction/2371728

反応式

関与物質

役割名称HCID仕込み量
反応物PhosgeneHCID 6371—
反応物Potassium CarbonateHCID 11430—
反応物3-(2-Chloro-4-fluorophenoxy)-1-(diphenylmethyl)azetidineHCID 15042226—
溶媒DichloromethaneHCID 6344—
生成物3-(2-Chloro-4-fluorophenoxy)-1-azetidinecarbonyl chlorideHCID 15042234—

反応条件

温度0 °C

反応手順

A stirred solution of 9.0 g (0.09 mole) of phosgene in 200 mL of methylene chloride under nitrogen was treated with 12.5 g (0.09 mole) of anhydrous potassium carbonate and stirred for 30 min. The reaction mixture was cooled in an ice bath while 28 g (0.08 mole) of 3-(2-chloro-4-fluorophenoxy)-1-(diphenylmethyl)azetidine in 100 mL of methylene chloride was added dropwise. After stirring for 16 hr at ambient temperature the reaction mixture was cooled to 0° C. in an ice water bath and small pieces of ice were added to destroy the excess phosgene, being careful to control the evolution of carbon dioxide gas. When the evolution of gas ceased, the reaction mixture was decanted from the inorganic slurry, dried (filtered through Whatman PS paper) and concentrated in vacuo, 41.9 g. Upon standing, a semisolid residue formed and the solid was collected by filtration after trituration with hexane to obtain 13.2 g (62.5%). A sample was recrystallized from hexane for analysis yielding fine white crystals, mp 93°-94° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05095014
出典データセットuspto-grants-1992_03
ORD IDord-4d6ddf24693243aebde1c9b1fa6f28f8
出典メモuspto-grants-1992_03