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HRID 1704326作成日:2026年10月27日

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/1704326

反応式

関与物質

役割名称HCID仕込み量
反応物7-Benzoyl-3-methyl-3-(methylsulfanyl)-1,3-dihydro-2H-indol-2-oneHCID 12909816—
溶媒TetrahydrofuranHCID 8028—
生成物7-Benzoyl-3-methyl-1,3-dihydro-2H-indol-2-oneHCID 1290124389%

反応手順

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 nickelwater 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 a 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04126635
出典データセットuspto-grants-1978_11
ORD IDord-ecc835171d4e47e59a71ca986af1d4bc
出典メモuspto-grants-1978_11