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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 442543생성일: 2026년 10월 26일

7-Benzoyl-3-methyl-3-(methylsulfanyl)-1,3-dihydro-2H-indol-2-one → 7-Benzoyl-3-methyl-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/442543

반응식

참여 물질

역할이름HCID투입량
반응물7-Benzoyl-3-methyl-3-(methylsulfanyl)-1,3-dihydro-2H-indol-2-oneHCID 12909816—
촉매Hydroxy-nickelHCID 444642—
용매TetrahydrofuranHCID 8028—
생성물7-Benzoyl-3-methyl-1,3-dihydro-2H-indol-2-oneHCID 1290124389%

반응 단계

A stirred solution of 8 g. (0.027 mole) of 7-benzoyl-3-methyl-3-methylthioindolin-2-one in 80 ml. of tetrahydrofuran was treated under N2 with 40 g. of a commercial Raney nickel-water mixture over a 2 hr. period. At the end of this period the mixture was filtered and the residue washed thoroughly with tetrahydrofuran. One drop of concentrated hydrochloric acid was added to the filtrate and the dark orange solution turned pale yellow. The solution was stripped under vacuum to yellow oil which crystallized on seeding. The material was recrystallized from toluene petroleum ether to give a white crystalline material. The solid (6.0 g., 89% yield) melted at 125°-127° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04045576
출처 데이터셋uspto-grants-1977_08
ORD IDord-297e996940294fc783e26797a5ab6bb2
출처 메모uspto-grants-1977_08