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HRID 1704322作成日:2026年10月27日

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

https://huagongshe.com/reaction/1704322

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TriethylamineHCID 8471—
反応物2-AminobenzophenoneHCID 76080—
反応物Tert-Butyl hypochloriteHCID 521297—
反応物Ethyl 2-(methylthio)propionateHCID 3016224—
溶媒DichloromethaneHCID 6344—
生成物7-Benzoyl-3-methyl-3-(methylsulfanyl)-1,3-dihydro-2H-indol-2-oneHCID 12909816—

反応手順

A stirred solution of 3.94 g. (0.02 mole) of 2-aminobenzophenone in methylene chloride at -65° C. was treated with 2.16 g. (0.02 mole) of t-butylhypochlorite. After 15 min. 2.96 g. ethyl α-(methylthio)propionate was added dropwise and stirring continued for 1 hr. At the end of this time 2.02 g. of triethylamine (0.02 mole) was added dropwise and the reaction solution was allowed to warm to room temperature. This was followed by treatment with 1N hydrochloric acid and stirred for 15 min. The methylene chloride solution was then separated and stripped under vacuum. The yellow oil residue was triturated with isopropyl ether and 3 g. of a yellow solid was filtered off (51%). Recrystallization from absolute ethanol gave a cream color solid, m.p. 135°-137° 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-cc7815a29a5e41afa3c599e914a94b74
出典メモuspto-grants-1978_11