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HRID 844441作成日:2026年10月25日

p-Toluidine → ethyl 3,5-dimethyl-1H-indole-2-carboxylate

https://huagongshe.com/reaction/844441

反応式

関与物質

役割名称HCID仕込み量
反応物p-ToluidineHCID 7813—
反応物Butanoic acid, 2-ethyl-3-oxo-, ethyl esterHCID 79065—
反応物4-Methylbenzenediazonium chlorideHCID 10329484—
反応物Sodium NitriteHCID 23668193—
溶媒Hydrochloric AcidHCID 313—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Sodium HydroxideHCID 14798—
生成物ethyl 3,5-dimethyl-1H-indole-2-carboxylateHCID 5111582—

反応条件

温度0 °C

反応手順

23.57 g of p-toluidine are placed in a mixture of 120 ml of water and 50 ml of concentrated HCl, followed by dropwise addition, at 0° C., of 15.4 g of NaNO2 in 40 ml of water and the mixture is left stirring for 20 minutes at 0° C. A solution of 32 g of ethyl 2-ethyl-3-oxobutyrate in 150 ml of EtOH and 150 ml of 20% NaOH solution are added, at −10° C., to the p-toluenediazonium chloride solution thus formed. After stirring for 30 minutes at −5° C., the mixture is acidified to pH=4 by addition of dilute HCl and one litre of water. On trituration, a red solid forms, which is filtered off and then dried in an oven at 40° C. This solid is taken up in 200 ml of absolute EtOH and 20 ml of concentrated H2SO4 and the mixture is then refluxed for 45 minutes. The reaction medium is poured into an ice/water mixture and filtered, the precipitate is then taken up in EtOAc and this solution is washed with water and dried over MgSO4. The residue is chromatographed on silica, eluting with a DCM/heptane mixture: m.p.=118° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06380230B1
出典データセットuspto-grants-2002_04
ORD IDord-2c6c1322cae14abc857b1427fcc79150
出典メモuspto-grants-2002_04