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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1375308생성일: 2026년 10월 26일

Dimethylformamide → 10-Ethylphenothiazine-3-carbaldehyde

https://huagongshe.com/reaction/1375308

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium HydroxideHCID 14797—
반응물Phosphorus oxychlorideHCID 24813—
반응물N-EthylphenothiazineHCID 219178—
생성물10-Ethylphenothiazine-3-carbaldehydeHCID 314330—

반응 단계

A 3.7 ml (0.04 mol) quantity of phosphorus oxychloride (from Aldrich) was added dropwise to 4.4 ml (0.06 mol) of dry dimethylformamide (DMF) at 0° C. under a nitrogen atmosphere. This solution was warmed up slowly to room temperature. Then 5 g (0.02 mol) of 10-ethylphenothiazine in dry DMF was added dropwise to the solution. The reaction mixture was heated at 80° C. for 24 hours and poured into ice water. The obtained solution was neutralized with potassium hydroxide until the pH reached 6–8. The product was extracted with chloroform. The chloroform extract was dried with anhydrous sodium sulfate, filtered and distilled. The product was recrystallized from methanol. The yield of 10-ethylphenothiazine-3-carbaldehyde was 3.7 g (66%). The product had a melting point of 94–95° C. (recrystallized from methanol). A 1H NMR spectrum yielded the following results: (100 MHz, CDCl3, δ, ppm): 1.50 (t, J=7.0 Hz, 3H, CH3); 4.02 (q, J=7.0 Hz, 2H, CH2); 6.95–6.39 (m, 5H, Ar), 7.52–7.70 (m, 2H, Ar), 9.83 (s, 1H, CHO).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07169520B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-47241199647d4ce089373cf99779e30a
출처 메모uspto-grants-2007_01