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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 268577생성일: 2026년 10월 25일

Dimethylformamide → 10-Ethylphenothiazine-3-carbaldehyde

https://huagongshe.com/reaction/268577

반응식

참여 물질

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

반응 단계

Phosphorus oxychloride (POCl3, 3.7 ml, 0.04 mol) (obtained 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. Next, a solution of 5 g (0.02 mol) of 10-ethylphenothiazine in dry DMF was added dropwise. The reaction mixture was refluxed at 80° C. for 24 hours and poured into the ice water. This solution was neutralized with potassium hydroxide until the pH reached 6-8. The product was extracted with chloroform. The chloroform extract was dried over anhydrous sodium sulfate, filtered and distilled. The product was recrystallized from methanol. The yield of 10-ethylphenothiazine-3-carbaldehyde (C15H13NOS, FW=255.34) was 3.7 g (66%). The melting point of the product (recrystallized from methanol) was 94-95° C. The 1H-NMR spectrum (100 MHz) of the product in CDCl3 was characterized by the following chemical shifts (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 번호US07445877B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-82e2035ccbc6486fafa9479cfcbc429d
출처 메모uspto-grants-2008_11