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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16629생성일: 2026년 10월 23일

2-Methyl-2-butene → 1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxylic acid

https://huagongshe.com/ko/reaction/16629

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-2-buteneHCID 10553—
반응물Monobasic potassium phosphateHCID 516951—
반응물1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxaldehydeHCID 2838253—
반응물Sodium ChloriteHCID 23668197—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매tert-ButanolHCID 6386—
생성물1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxylic acidHCID 58944728101.1%

반응 단계

To a suspension of 1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxaldehyde (Compound 50, 150 mg, 0.51 mmol) in acetonitrile (6 ml), tert-butanol (6 ml) and H2O (6 ml) was added 2-methyl-2-butene (4 ml), potassium phosphate monobasic (1.4 g, 10.2 mmol), sodium chlorite (80%, 1.15 g, 10.2 mmol). The mixture was stirred at room temperature for 20 h, more potassium phosphate monobasic (0.35 g, 2.6 mmol) and sodium chlorite (80%, 0.29 g, 2.6 mmol) were added and stirred at room temperature for 24 h. The solvent was removed under reduced pressure. The residue solid was washed with H2O (×3) and filtered, dissolved in acetone and filtered to yield 1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxylic acid (Compound 51) as a yellow powder (160 mg, 100%). 1H-NMR (ACETONE-d6) δ 2.83 (s, 3 H), 5.68 (s, 2 H), 7.06-7.15 (m, 2 H), 7.25-7.41 (m, 3 H), 7.68 (d, J=9.1 Hz, 1 H), 8.10 (dd, J =9.1, 2.3 Hz, 1 H), 9.11 (d, J=2.3 Hz, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737173B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-7a744141b8f04f279f740449c088f55b
출처 메모uspto-grants-2010_06