돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 353602생성일: 2026년 10월 24일

Ammonium Chloride → 3-Chloromethyl-4-(4-fluoro-benzoyl)-benzonitrile

https://huagongshe.com/ko/reaction/353602

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물2-(Chloromethyl)-4-cyanobenzoyl chlorideHCID 11344910—
반응물Ethyl acetate hexaneHCID 21226206—
반응물HCID 178418676HCID 178418676—
용매TetrahydrofuranHCID 8028—
생성물3-Chloromethyl-4-(4-fluoro-benzoyl)-benzonitrileHCID 9943434—

반응 단계

A solution of 4-fluoro phenylmagnesium bromide (3.76 g) in tetrahydrofuran (15 ml) was added to a cooled solution of 2-chloromethyl-4-cyano-benzoyl chloride (3.95 g) in tetrahydrofuran (10 ml) so that the temperature did not raise above 0° C. The mixture was warmed slowly to room temperature and stirred over night. Saturated ammonium chloride solution (60 ml) was added and stirring continued for 0.5 hours. The phases were separated and the aqueous phase was extracted with diethylether (30 ml). The combined organic phases were dried over sodium sulfate, filtered and dried in vacuo to give a brown solid. Flash chromatography (ethyl acetate/n-hexane=1/10) provided the product as colourless solid. Yield 2.95 g, 58%. 1H NMR (CDCl3, 400 MHz): 4.71 (2H, s), 7.16-7.21 (2H, m), 7.46 (1H, d, J=7.9 Hz), 7.71 (1H, dd, J=1.5, 7.9 Hz), 7.81-7.86 (2H, m), 7.89 (1H, d, J=1.5 Hz). 13C NMR (CDCl3, 100 MHz): 42.3, 115.0, 116.4, 116.6, 117.9, 129.6, 132.95, 132.98, 133.4, 133.5, 134.3, 138.7, 142.4, 165.5, 168.1, 194.5.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06753433B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-e922eef638ad42aaa2bcc784d588c265
출처 메모uspto-grants-2004_06