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HRID 2051870作成日:2026年10月25日

4-Benzoyl-3-(methylsulfanyl)-1,3-dihydro-2H-indol-2-one → 4-Benzoyl-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/2051870

反応式

関与物質

役割名称HCID仕込み量
反応物4-Benzoyl-3-(methylsulfanyl)-1,3-dihydro-2H-indol-2-oneHCID 12923552—
触媒NickelHCID 935—
溶媒TetrahydrofuranHCID 8028—
生成物4-Benzoyl-1,3-dihydro-2H-indol-2-oneHCID 12901246—

反応手順

A stirred suspension of 7.0 g. (0.0248 mole) of 4-benzoyl-3-methylthioindolin-2-one in 400 ml. of tetrahydrofuran was treated portionwise under a nitrogen atmosphere with 35.0 g. of Raney nickel over a 2.5 hr. period. The reaction mixture was stirred for 1.5 hr. after addition as complete and the catalyst removed by filtration. The filter cake was washed well with tetrahydrofuran and methylene chloride and the filtrate evaporated under reduced pressure. The residue (5.6 g.) was recrystallized from methanol and gave 4.45 g. (76%) of product m.p. 210°-212° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04182774
出典データセットuspto-grants-1980_01
ORD IDord-8f29148ff5eb4c049af611e61c24d96b
出典メモuspto-grants-1980_01