戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1242135作成日:2026年10月25日

4-Ethylbenzoic Acid → Methyl 3-methyl-1H-indole-6-carboxylate

https://huagongshe.com/reaction/1242135

反応式

関与物質

役割名称HCID仕込み量
反応物4-Ethylbenzoic AcidHCID 12086—
反応物Dimethylformamide dimethyl acetalHCID 78373—
反応物Methyl 4-ethyl-3-nitrobenzoateHCID 21938352—
溶媒DimethylformamideHCID 6228—
生成物Methyl 3-methyl-1H-indole-6-carboxylateHCID 21938240—

反応条件

温度130 °C

反応手順

Methyl 4-ethyl-3-nitrobenzoate (5.0 g), which had been prepared through nitration followed by methyl-esterification of 4-ethylbenzoic acid, is dissolved in N,N-dimethylformamide (50 ml), to which is added N,N-dimethylformamide dimethyl acetal (8.45 g), and stirred under heat at 130° C. for 3 hours. The reaction mixture is concentrated under reduced pressure, and the resulting red oily residue is dissolved in methanol (50 ml), to which is added palladium-carbon (5%, 0.400 g), and stirred in a hydrogen atmosphere at room temperature for 2.5 hours. Then, this is further stirred at 50° C. for 2 hours and thereafter at room temperature for 3 days. The catalyst is removed through filtration, and the filtrate is concentrated under reduced pressure. The resulting residue is recrystallized from t-butyl methyl ether to obtain a pale yellow crystal of the intended product (2.4 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07115647B2
出典データセットuspto-grants-2006_10
ORD IDord-356be7b1a1e84db4bfec2619f722bea0
出典メモuspto-grants-2006_10