돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2427717생성일: 2026년 10월 27일

7-Methyl-1-oxo-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-1H-isoindole-5-carbonitrile → 5-Aminomethyl-7-methyl-2-(4-trifluoromethoxybenzyl)-2,3-dihydroisoindol-1-one

https://huagongshe.com/reaction/2427717

반응식

참여 물질

역할이름HCID투입량
반응물7-Methyl-1-oxo-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-1H-isoindole-5-carbonitrileHCID 57949363—
촉매NickelHCID 935—
용매EthanolHCID 702—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ammonium HydroxideHCID 14923—
생성물5-Aminomethyl-7-methyl-2-(4-trifluoromethoxybenzyl)-2,3-dihydroisoindol-1-oneHCID 57949320—

반응 단계

A solution of 7-methyl-1-oxo-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-1H-isoindole-5-carbonitrile (0.104 g, 0.3 mmol) in THF (1 mL) and ethanol (4 mL) was treated with a suspension of Raney nickel in water (1 mL) and aqueous NH4OH (0.5 mL). The mixture was stirred at ambient temperature for 12 h under hydrogen atmosphere (1 atm.). After this time GC-MS indicated that all the starting material was consumed. The reaction mixture was filtered and concentrated to afford the desired product. The material was used without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07968570B2
출처 데이터셋uspto-grants-2011_06
ORD IDord-d9e73f0acdaf49be8303457ad70748c1
출처 메모uspto-grants-2011_06