戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 74465作成日:2026年10月24日

Ethyl Propionate → 5-bromo-1-(toluene-4-sulfonyl)-6-trifluoromethyl-1H-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/ja/reaction/74465

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl PropionateHCID 7749—
反応物DiisopropylethylamineHCID 81531—
反応物N-(4-bromo-2-iodo-5-trifluoromethyl-phenyl)-4-methyl-benzenesulfonamideHCID 68005027—
触媒Zinc bromideHCID 10421208—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
生成物5-bromo-1-(toluene-4-sulfonyl)-6-trifluoromethyl-1H-indole-2-carboxylic acid ethyl esterHCID 68004700—

反応条件

温度80 °C

反応手順

N,N-diisopropylethyl amine (0.42 ml, 2.4 mmol), ethyl propionate (0.12 ml, 1.2 mmol), and tetrakis(triphenylphosphine)palladium (46 mg, 0.04 mmol) were added to an anhydrous tetrahydrofuran (THF) solution (3.2 ml) containing N-(4-bromo-2-iodo-5-trifluoromethyl-phenyl)-4-methyl-benzenesulfonamide (208 mg, 0.4 mmol) and zinc bromide (270 mg, 1.2 mmol). Then, the mixture was evacuated, and backfilled with argon. This was stirred at 80° C. for 13 hours. After cooling it to room temperature, the reaction mixture was filtered through Celite, and washed with ethyl acetate. The wash solution was washed with an aqueous solution saturated with sodium bicarbonate and an aqueous solution saturated with sodium chloride, and dried over anhydrous sodium sulfate. The desiccant was removed by filtration, and concentration was performed. Then, the residue obtained by concentration under reduced pressure was purified by silica gel column chromatography. Thus, 5-bromo-1-(toluene-4-sulfonyl)-6-trifluoromethyl-1H-indole-2-carboxylic acid ethyl ester was obtained as a pale brown solid (195 mg, 50%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829199B2
出典データセットuspto-grants-2014_09
ORD IDord-bd000ac9664b45088171998e60399da1
出典メモuspto-grants-2014_09