돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1364555생성일: 2026년 10월 24일

4-(Methylsulfonyl)-3-(trifluoromethyl)benzonitrile → [4-Methanesulfonyl-3-(trifluoromethyl)phenyl]methanamine

https://huagongshe.com/ko/reaction/1364555

반응식

참여 물질

역할이름HCID투입량
반응물4-(Methylsulfonyl)-3-(trifluoromethyl)benzonitrileHCID 45933716—
촉매NickelHCID 935—
용매AmmoniaHCID 222—
용매MethanolHCID 887—
생성물[4-Methanesulfonyl-3-(trifluoromethyl)phenyl]methanamineHCID 66632608—

반응 단계

A mixture of 4-fluoro-3-trifluoromethylbenzonitrile (75 mg, 0.40 mmol), sodium sulfinate (44.5 mg, 0.44 mmol) in N,N-dimethylformamide (1.5 mL) was heated at 100° C. for 2 h. The reaction mixture was cooled to room temperature, quenched with water. The resulting white solid was collected via filtration, washed with cold water, dried in a vacuum oven to give 4-methanesulfonyl-3-trifluoromethyl-benzonitrile (90 mg, 90% yield). This benzonitrile was hydrogenated in 2N NH3 in methanol with 35 mg of Raney Ni under a hydrogen balloon for 2 h. The reaction mixture was filtered through a celite plug, washed with methanol, evaporated in vacuo to give the titled compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07888374B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-f6a0f34fb0a64f62a97a309ec3886341
출처 메모uspto-grants-2011_02