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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2380139생성일: 2026년 10월 25일

Acetic Anhydride → 6,12,18-Tris(benzyloxy)-7,13,19-trioxo-6,12,18-triazaeicosanenitrile

https://huagongshe.com/reaction/2380139

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물6,12,18-Tris(benzyloxy)-7,13-dioxo-6,12,18-triazaoctadecanenitrileHCID 9986266—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물6,12,18-Tris(benzyloxy)-7,13,19-trioxo-6,12,18-triazaeicosanenitrileHCID 1010083860%

반응 조건

온도0 °C

반응 단계

Acetic anhydride (8 mL) was slowly added to a solution of (8) (1.25 g, 2.03 mmol) in pyridine (50 mL) and CH2Cl2 (30 mL) which had been cooled to 0° C. Stirring was continued at 0° C. for 30 minutes and then at room temperature overnight. Solvents were removed under high vacuum, and the residue was dissolved in CHCl3 (120 mL), followed by washing with 0.5N HCl (2×40 mL) and saturated NaHCO3 (2×40 mL). After solvent removal, the crude oil was purified by silica gel column chromatography, eluting with 3:1 EtOAc/hexane, to furnish 0.8 g (60%) of (9) as an oil: NMR δ 1.40-1.80 (m, 12H), 2.05 (s, 3H), 2.20-2.50 (m, 6H), 3.40-3.73 (m, 6H), 4.75 (s, 6H), 7.32 (s, 15H). Anal. (C38H 48 N4O6) C, H, N.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05364965
출처 데이터셋uspto-grants-1994_11
ORD IDord-a9836b582aa54a22abdf29847f3dc11d
출처 메모uspto-grants-1994_11