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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 268576생성일: 2026년 10월 26일

Iodoethane → N-Ethylphenothiazine

https://huagongshe.com/reaction/268576

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물PhenothiazineHCID 7108—
반응물Potassium HydroxideHCID 14797—
촉매Tetrabutylammonium hydrogen sulfateHCID 94433—
용매TolueneHCID 1140—
생성물N-EthylphenothiazineHCID 219178—

반응 단계

A mixture of 10 g (0.05 mol) of phenothiazine (obtained from Fluka), 11.7 g (0.075 mol) of iodoethane (obtained from Aldrich), 4.2 g (0.075 mol) of potassium hydroxide and 0.25 g of tetra-n-butylammonium hydrogen sulfate (obtained from Aldrich) in 200 ml of dry toluene was refluxed for 24 hours. After cooling, the reaction mixture was filtered and the solvent was evaporated. The product was recrystallized from methanol. The yield of 10-ethylphenothiazine (C14H13NS, FW=227.33) was 90%. The melting point of the product was 103-104° C. The 1H-NMR spectrum (100 MHz) of the product in CDCl3 was characterized by the following chemical shifts (δ, ppm): 1.40 (t, J=7.0 Hz, 3H, CH3); 3.90 (q, J=7.0 Hz, 2H, CH2); 6.78-7.32 (m, 8H, Ar).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07445877B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-5dca1ffcee9c4e1fac40ef9667593d59
출처 메모uspto-grants-2008_11