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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2191197생성일: 2026년 10월 26일

Iodine → 1-Butyl-4-(3-(dodecyloxy)-3-oxopropyl)-1-methylpiperazin-1-ium bromide

https://huagongshe.com/reaction/2191197

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물IsopropanolHCID 3776—
반응물Butyl bromideHCID 8002—
반응물Dodecyl 3-(4-methylpiperazin-1-yl)propanoateHCID 59270650—
용매Toluene methanolHCID 21867641—
생성물1-Butyl-4-(3-(dodecyloxy)-3-oxopropyl)-1-methylpiperazin-1-ium bromideHCID 66704700—

반응 단계

In a 100-mL round bottom flask, 5.0 g (0.015 moles) of dodecyl 3-(4-methylpiperazin-1-yl)propanoate and 7.3 g (0.044 moles) of butyl bromide are combined with 10 mL of isopropyl alcohol. This solution is heated to reflux overnight. Thin layer chromatography (TLC) was used to monitor the progress of the reaction with 1:1 methanol/toluene as a mobile phase and iodine to reveal the components on the plate. After the reaction is complete, the solvent and excess of butyl bromide are evaporated under vacuum. Finally, the resulting solid is dried under vacuum at 120° C. 1H-NMR (300 MHz, CDCl3): δ 3.92 (t, 5.9 Hz, 2H), 3.76 (m, 2H), 3.56 (m, 4H), 3.35 (s, 3H), 2.91 (m, 6H), 2.46 (t, 6.6 Hz, 2H), 1.67 (m, 2H), 1.47 (m, 2H), 1.12 (m, 24H), 0.74 (m, 6H). 13C-NMR (75 MHz, CDCl3): δ 170.98, 64.61, 59.14, 51.84, 45.88, 31.44, 31.28, 30.81, 29.18, 29.16, 29.13, 29.08, 28.87, 28.81, 28.11, 25.50, 25.43, 22.21, 21.96, 21.60, 13.66, 13.49.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08329620B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-e0a98524da184b9f80b78cd00443c372
출처 메모uspto-grants-2012_12