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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50562생성일: 2026년 10월 27일

Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- → (2E)-3-(6-Quinoxalinyl)-2-propenal

https://huagongshe.com/reaction/50562

반응식

참여 물질

역할이름HCID투입량
반응물Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
반응물Quinoxaline-6-carboxaldehydeHCID 763958—
반응물(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromideHCID 2724194—
용매DichloromethaneHCID 6344—
용매Potassium CarbonateHCID 11430—
생성물(2E)-3-(6-Quinoxalinyl)-2-propenalHCID 2263079965.1%

반응 단계

A mixture of 6-quinoxalinecarboxaldehyde (0.62 g, 3.92 mmol, prepared as described in Photochem. Photobiol. 1991, 54, 7), (1,3-dioxolan-2-ylmethyl)triphenylphosphonium bromide (2.50 g, 5.82 mmol), and TDA-1 (1.20 mL, 3.75 mmol) in dichloromethane (20 mL) and sat. aq. K2CO3 (20 mL) was heated to reflux for 4 h. The layers were separated and the aqueous layer was extracted with dichloromethane (2×20 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried (Na2SO4), and concentrated. THF (10 mL) and 10% HCl (10 mL) were added and the mixture was stirred for 1 h at rt. The mixture was cooled to 0° C., the precipitated solids were removed by filtration, washed with water and dried in vacuo to give 0.47 g (65%) of the title compound as a tan solid. MS 185 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713455B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-d7424d04e2f24310a1dbd88da33e8436
출처 메모uspto-grants-2004_03