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HRID 844441생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/844441

반응식

참여 물질

역할이름HCID투입량
반응물p-ToluidineHCID 7813—
반응물Butanoic acid, 2-ethyl-3-oxo-, ethyl esterHCID 79065—
반응물4-Methylbenzenediazonium chlorideHCID 10329484—
반응물Sodium NitriteHCID 23668193—
용매Hydrochloric AcidHCID 313—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Sodium HydroxideHCID 14798—
생성물ethyl 3,5-dimethyl-1H-indole-2-carboxylateHCID 5111582—

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06380230B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-2c6c1322cae14abc857b1427fcc79150
출처 메모uspto-grants-2002_04