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HRID 267915作成日:2026年10月27日

1,2-Dichloroethane → HCID 178423700、化合物

https://huagongshe.com/reaction/267915

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物PhenothiazineHCID 7108—
反応物Potassium HydroxideHCID 14797—
反応物Phosphorus oxychlorideHCID 24813—
反応物5-Methyl-2-pyrrolidoneHCID 66055—
生成物HCID 178423700HCID 17842370017%

反応手順

A mixture of 5-methyl-2-pyrrolidinone (6.0 g., 0.06 mole), phosphorus oxychloride (9.2 g., 0.06 mole) in 60 ml. of 1,2-dichloroethane is refluxed for 10 min. A solution of phenothiazine (6.0 g., 0.03 mole) in 20 ml. of 1,2-dichloroethane is added at the end of the reflux period and the reaction mixture stirred and refluxed for 20 hr., and then poured onto 20 ml. of 5N potassium hydroxide and 20 g. of crushed ice. The 1,2-dichloroethane layer is separated and extracted with 30 ml. of 1.5N hydrochloric acid and 30 ml. of water removing water soluble by-product 10-[2-(5-methyl-1-pyrrolinyl)]-phenothiazine hydrochloride. After drying the 1,2-dichloroethane solution over magnesium sulfate, the 1,2-dichloroethane solution is concentrated and the solid thus obtained stirred with 40 ml. of acetone and filtered. Crystallization of the filtercake from ethanol-ether provides analytically pure 10-[5-METHYL-1-(5-METHYL-1 -PYRROLIN-2-YL]PHENOTHIAZINE HYDROCHLORIDE in a yield of 17%, m.p. 257°-264° C. (corr.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03946004
出典データセットuspto-grants-1976_03
ORD IDord-be28f5f9e3d545928b4392e148b1dfae
出典メモuspto-grants-1976_03