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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1657752생성일: 2026년 10월 25일

Oxalic Acid → 1,10-Dimethyl-3,4-dihydro-1H-1,4-oxazino[4,3-a]indole-1-propionaldehyde

https://huagongshe.com/reaction/1657752

반응식

참여 물질

역할이름HCID투입량
반응물Oxalic AcidHCID 971—
반응물PyridineHCID 1049—
반응물Trifluoroacetic acidHCID 6422—
반응물1,10-Dimethyl-3,4-dihydro-1H-1,4-oxazino[4,3-a]indole-1-propanolHCID 21389553—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물1,10-Dimethyl-3,4-dihydro-1H-1,4-oxazino[4,3-a]indole-1-propionaldehydeHCID 21389566—

반응 단계

N,N-Dicyclohexylcarbodiimide (2.87 g.) is added to a cooled, stirred solution of the primary alcohol, 1,10-dimethyl-3,4-dihydro-1H-1,4-oxazino[4,3-a]indole-1-propanol (1.0 g.), described in Example 462, in 10 ml. of dimethyl sulfoxidebenzene (2:1) containing trifluoroacetic acid (0.18 ml.) and pyridine (0.38 ml.). The reaction is stirred at room temperature under nitrogen for 5 hr. The reaction mixture is now diluted with 100 ml. of ether, followed by the dropwise addition of a solution of oxalic acid (1.26 g.) in 6 ml. of methanol. After thirty minutes, water (100 ml.) is added and the insoluble material is collected. The organic phase is washed with water (2X), 5% aqueous sodium bicarbonate (2X) and water (2X). After drying (MgSO4) the organic phase is evaporated to yield an oil. The oil is purified by chromatography on silica gel. Elution with 10% ether in benzene affords the title compound as an oil, δCHCl3Max 1720 cm-1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03962236
출처 데이터셋uspto-grants-1976_06
ORD IDord-f08501c0861640989f2436350b746b07
출처 메모uspto-grants-1976_06