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HRID 268576作成日:2026年10月26日

Iodoethane → N-Ethylphenothiazine

https://huagongshe.com/reaction/268576

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 (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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07445877B2
出典データセットuspto-grants-2008_11
ORD IDord-5dca1ffcee9c4e1fac40ef9667593d59
出典メモuspto-grants-2008_11