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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 381766생성일: 2026년 10월 26일

tert-Butanol → 2-(2-oxo-1,2-dihydro-3-quinolinyl)-1H-indole-5-carboxylic acid

https://huagongshe.com/reaction/381766

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물2-Methyl-1-buteneHCID 11240—
반응물5-Formyl-2-(2-oxo-1,2-dihydro-quinolin-3-yl)-indole-1-carboxylic acid tert-butyl esterHCID 12111689—
반응물Sodium ChloriteHCID 23668197—
반응물Monosodium phosphateHCID 23672064—
용매TetrahydrofuranHCID 8028—
생성물2-(2-oxo-1,2-dihydro-3-quinolinyl)-1H-indole-5-carboxylic acidHCID 22668254—

반응 단계

A solution of 2-(2-oxo-1,2-dihydro-3-quinolinyl)i1H-indole-5-carbaldehyde (5-8, 500 mg, 1.29 mmol, 1 equiv) in a 4:1 mixture of THF and t-BuOH was treated with 2 -methyl butene (8 mL), an aqueous solution of sodium phosphate monobasic (0.14 M 355.2 mg, 2.57 mmol, 2.00 equiv), and sodium chlorite (232.8 mg, 2.57 mmol, 2.00 equiv). Additional solid sodium phosphate monobasic (380 mg, 2.76 mmol, 2.14 equiv) and sodium chlorite (300 mg, 3.32 mmol, 2.57 equiv) was added in 2 equal portions over 2.5 h. The reaction mixture was concentrated, and the residue dissolved in EtOAc (60 mL), then washed twice with a 25:1 mixture of aqueous 10% sodium bisulfite solution and 10% potassium hydrogen sulfate solution (2×50 mL). The organic layer was dried over sodium sulfate, concentrated, and combined with a precipitate in the aqueous layer which was filtered and dried to 2-(2-oxo-1,2-dihydro-3-quinolinyl)-1H-indole-5-carboxylic acid (6-1) as an off-white solid. 1H NMR (500 MHz, DMSO) δ12.13 (s, 1H), 8.27 (s, 1H), 8.14 (m, 3H), 7.95 (d, 1H, J=7.8 Hz), 7.76 (d, 1H, J=7.8 Hz), 7.54 (t, 1H, J=7.8), 7.36 (d, 1H, J=7.8), 7.24 (t, 1H, J=7.8) 1.36 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06306874B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-34b9e7618b89497b8757735dccc7a32d
출처 메모uspto-grants-2001_10