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HRID 1375307作成日:2026年10月27日

Iodoethane → N-Ethylphenothiazine

https://huagongshe.com/reaction/1375307

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物PhenothiazineHCID 7108—
反応物Potassium HydroxideHCID 14797—
触媒Tetrabutylammonium hydrogen sulfateHCID 94433—
溶媒TolueneHCID 1140—
生成物N-EthylphenothiazineHCID 219178—

反応手順

A mixture of 10 g (0.05 mol) of phenothiazine (from Fluka), 11.7 g (0.075 mol) of iodoethane (from Aldrich), 4.2 g (0.075 mol) of potassium hydroxide, and 0.25 g of tetra-n-butylammonium hydrogen sulfate (from Aldrich) in 200 ml of dry toluene was refluxed for 24 hrs. The cooled reaction mixture was filtered and the solvent was evaporated. The product was recrystallized from methanol. The yield of 10-ethylphenothiazine was 10.2 g (90%). The product had a melting point of 103–104° C. (recrystallized from methanol). A 1H NMR spectrum yielded the following results (100 MHz, CDCl3, 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07169520B2
出典データセットuspto-grants-2007_01
ORD IDord-243b4f4bd18e4e9b86c3f72c39e5d38d
出典メモuspto-grants-2007_01