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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 363386생성일: 2026년 10월 25일

Bis(3-aminopropyl)amine → Bis(3-{[(4-methylphenyl)sulfonyl]amino}propyl)[(4-methylphenyl)sulfonyl]amine

https://huagongshe.com/reaction/363386

반응식

참여 물질

역할이름HCID투입량
반응물Bis(3-aminopropyl)amineHCID 5942—
반응물4-Toluenesulfonyl chlorideHCID 7397—
용매PyridineHCID 1049—
생성물Bis(3-{[(4-methylphenyl)sulfonyl]amino}propyl)[(4-methylphenyl)sulfonyl]amineHCID 37379759%

반응 단계

To a stirred solution of p-toluenesulfonyl chloride (240 g, 1.26 mole) in pyridine (600 ml) at 0° C. was added a solution of 1,5,9-triazanonane (50.0 g, 0.381 mole) in pyridine (100 ml) under a dry nitrogen atmosphere, maintaining the temperature ≤60° C. The addition required 15 minutes. The solvent was removed in vacuo and the resulting yellow oil was dissolved in ethyl acetate (1 l) and H2O (500 ml). The ethyl acetate layer was separated, washed with 0.1N HCl, H2O and saturated NaCl solution and dried (MgSO4). The solution was decolorized with silica gel and the solvent was removed in vacuo to give 133 g (59% yield) of the crude product as a glassy solid: 1H NMR (CDCl3) δ 1.71 (quint, J=6.6 Hz, 4 H), 2.42 (s, 6 H), 2.43 (s, 3 H), 2.96 (quart, J=6.4 Hz, 4 H), 3.11 (t, J=6.8 Hz, 4 H), 5.12 (t, J=6.6 Hz, 2 H), 7.30 (m, 6 H), 7.63 (m, 2 H), 7.73 (m, 4 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05874421
출처 데이터셋uspto-grants-1999_02
ORD IDord-74d5eaa312b44262b58faba2559a5680
출처 메모uspto-grants-1999_02