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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2371728생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2371728

반응식

참여 물질

역할이름HCID투입량
반응물PhosgeneHCID 6371—
반응물Potassium CarbonateHCID 11430—
반응물3-(2-Chloro-4-fluorophenoxy)-1-(diphenylmethyl)azetidineHCID 15042226—
용매DichloromethaneHCID 6344—
생성물3-(2-Chloro-4-fluorophenoxy)-1-azetidinecarbonyl chlorideHCID 15042234—

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05095014
출처 데이터셋uspto-grants-1992_03
ORD IDord-4d6ddf24693243aebde1c9b1fa6f28f8
출처 메모uspto-grants-1992_03