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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 403608생성일: 2026년 10월 24일

3H-Indole, 2,3,3-trimethyl- → 2,3,3-trimethyl-1-(3-triethylammoniopropyl)-3H-indolium bromide chloride

https://huagongshe.com/ko/reaction/403608

반응식

참여 물질

역할이름HCID투입량
반응물3H-Indole, 2,3,3-trimethyl-HCID 15427—
반응물N-(3-bromopropyl)triethylammonium chlorideHCID 89781116—
생성물2,3,3-trimethyl-1-(3-triethylammoniopropyl)-3H-indolium bromide chlorideHCID 8978158036%

반응 조건

온도140 °C

반응 단계

Freshly distilled 2,3,3-trimethylindolenine (0.53 g, 3.3 mmol) and N-(3-bromopropyl)triethylammonium chloride (1.01 g, 3.9 mmol) were mixed in the thick-wall tube and placed under an argon atmosphere. The mixture was then heated at 140° C. for 1.5 h, giving a deep red viscous product, which solidified to a glass on cooling. It was ground to a powder under acetone; product was collected by filtration, triturated 3 times with 10 mL portions of acetone and dried under vacuum to give 0.45 g (36%) of 2,3,3-trimethyl-1-(3-triethylammoniopropyl)-3H-indolium bromide chloride as a white powder. δH (200 MHz, DMSO-d6) 8.10 (1H, d, 6.7 Hz, arom.), 7.87 (1H, d, 5.8 Hz, arom.), 7.75-7.58 (2H, m, arom.), 4.56 (2H, t, 7.3 Hz, N+CH2), 3.27 (6H, q, 6.0 Hz, N+(CH2)3), 2.91 (3H, s, CH3), 2.34-2.10 (2H, m, N+CH2), 1.56 (6H, s, (CH3)2) 1.36-1.05 (11H, m, CH2, (CH3)3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748446B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-42be14ad864246099ad5c240b809973e
출처 메모uspto-grants-2014_06