돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72658생성일: 2026년 10월 26일

2,4,6-Trimethoxybenzaldehyde → (E)-2-methoxy-3-nitro-5-((2,4,6-trimethoxystyrylsulfinyl)methyl)pyridine

https://huagongshe.com/reaction/72658

반응식

참여 물질

역할이름HCID투입량
반응물2,4,6-TrimethoxybenzaldehydeHCID 70019—
반응물2-((6-Methoxy-5-nitropyridin-3-yl)methylsulfinyl)acetic acidHCID 67995981—
촉매PiperidineHCID 8082—
용매PyridineHCID 1049—
생성물(E)-2-methoxy-3-nitro-5-((2,4,6-trimethoxystyrylsulfinyl)methyl)pyridineHCID 5659865710%

반응 단계

A solution of 2-((6-methoxy-5-nitropyridin-3-yl)methylsulfinyl)acetic acid (0.15 g, 0.5 mmol) in dry pyridine (20 mL) was treated with 2,4,6-trimethoxybenzaldehyde (0.20 g, 1 mmol) and piperidine (10 drops). The mixture was refluxed for 2-3 hrs. The mixture was evaporated and the residue was purified by flash chromatography; yield 10%; 1H-NMR (CDCl3): δ 3.83 (s, 6H, OCH3), 3.83 (s, 3H, OCH3), 3.89 (1H, CH), 4.07 (1H, CH), 4.09 (s, 3H, OCH3), 6.09 (s, 2H, Ph-H), 6.97 (d, 1H, J=15.2 Hz, CH), 7.28 (d, 1H, J=15.2 Hz, CH), 8.19 (d, 1H, J=2.3 Hz, Py-H), 8.29 (d, 1H, J=2.3 Hz, Py-H). HR-MS (ESI+) m/z 408.8426 C18H20N2O7S requires 408.0991.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829003B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d5e3a9b867dc4d21bd8a50d6f2f332dd
출처 메모uspto-grants-2014_09