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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1372715생성일: 2026년 10월 23일

Methyl iodide → 1,2-Dimethylindole-3-carboxylic acid

https://huagongshe.com/ko/reaction/1372715

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물DiisopropylamineHCID 7912—
반응물1-Methylindole-3-carboxylic acidHCID 854040—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물1,2-Dimethylindole-3-carboxylic acidHCID 276103210%

반응 조건

온도-78 °C

반응 단계

Diisopropylamine (2.83 ml, 20.0 mmol) was dissolved in THF (35 ml). Under stirring at −78° C., n-butyl lithium (12.7 ml, 20.0 mmol, a 1.57M hexane solution) was added to the resulting solution. After stirring at 0° C. for 15 minutes, the reaction mixture was cooled again to −78° C. Under stirring, a solution of 1-methyl-1H-indole-3-carboxylic acid (1.75 g, 10.0 mmol) in THF (5 ml) was added. After the reaction mixture was stirred at the same temperature for 30 minutes, methyl iodide (3.42 ml, 55.0 mmol) was added. The reaction mixture was caused to rise back to room temperature over 30 minutes. The reaction mixture was poured into water and the mixture was stirred for 18 hours at room temperature. The reaction mixture was washed with ether. The water layer was acidified with 1M HCl, followed by extraction with ether. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by silica gel chromatography (middle pressure, linear gradient of chloroform/methanol from 10:0 to 20:1, 20 ml/min, φ 50×300 mm) to give 1,2-dimethyl-1H-indole-3-carboxylic acid (180 mg, 10%) as a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07157487B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-4f8cd2c46bde453a90ac695006c7cd31
출처 메모uspto-grants-2007_01