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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42512생성일: 2026년 10월 24일

Sodium Hydroxide → 6-bromo-1-cyclopropyl-1H-indole-4-carboxylic acid

https://huagongshe.com/ko/reaction/42512

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물methyl 6-bromo-1-cyclopropyl-1H-indole-4-carboxylateHCID 67467490—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물6-bromo-1-cyclopropyl-1H-indole-4-carboxylic acidHCID 6746513490%

반응 단계

To a solution of methyl 6-bromo-1-cyclopropyl-1H-indole-4-carboxylate (0.43 g, 1.462 mmol) in MeOH (12 mL) and THF (3 mL) was added 3 M NaOH (1.949 mL, 5.85 mmol). The reaction was stirred for 18 h at RT, at which time the volatiles were removed in vacuo. The residue was diluted with water and slowly acidifed with 1 N HCl to pH 4-5, then extracted with EtOAc (2×). The combine organics werewash with brine, dried over magnesium sulfate, filtered, and concentrated to give 6-bromo-1-cyclopropyl-1H-indole-4-carboxylic acid (0.376 g, 1.315 mmol, 90% yield) as a pale yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.92-1.01 (m, 2H) 1.05-1.12 (m, 2H) 3.51 (tt, J=7.07, 3.66 Hz, 1H) 6.89 (d, J=2.53 Hz, 1H) 7.52 (d, J=3.03 Hz, 1H) 7.80 (d, J=1.77 Hz, 1H) 7.99 (d, J=1.01 Hz, 1H) 13.05 (br. s., 1H). MS (ES) [M+H]+ 280.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536179B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-32f8c43d5409451fa8145c120cf44e46
출처 메모uspto-grants-2013_09