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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 963652생성일: 2026년 10월 25일

Toluene → 2-[5-(Benzyloxy)-2-nitroanilino]propionaldehyde dimethyl acetal

https://huagongshe.com/reaction/963652

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Potassium CarbonateHCID 11430—
반응물2,2-Dimethoxy-1-methylethylamineHCID 93658—
반응물4-(Benzyloxy)-2-chloro-1-nitrobenzeneHCID 819861—
용매Dimethyl SulfoxideHCID 679—
생성물2-[5-(Benzyloxy)-2-nitroanilino]propionaldehyde dimethyl acetalHCID 19083116—

반응 단계

A mixture of benzyl 3-chloro-4-nitrophenyl ether (48.2 g, 0.183 mole), 2-aminopropionaldehyde dimethyl acetal (65.3 g, 0.55 mole), potassium carbonate (101 g, 0.73 mole) and toluene in dry dimethyl sulfoxide, under nitrogen, is stirred at 99°-105° C. for 20 hours, cooled to room temperature and filtered. The filter cake is washed with ether. The combined filtrates are mixed with ice water. The phases are separated and the aqueous phase is extracted with ether. The ether extracts are combined with the organic phase. The combined organic phase is washed with six portions of water, dried (Na2SO4) and concentrated in vacuo to give an oil residue which is crystallized in methanol to afford the title product as a yellow solid, 39.6 g (64.5%). A sample is recrystallized from methanol to afford a yellow solid, mp 57°-62° C., identified by elemental and NMR analyses.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05763615
출처 데이터셋uspto-grants-1998_06
ORD IDord-18fc9b6dbc484a6e8834325bb1a74df5
출처 메모uspto-grants-1998_06