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HRID 893987作成日:2026年10月25日

Epichlorohydrin → HCID 21162606、化合物

https://huagongshe.com/reaction/893987

反応式

関与物質

役割名称HCID仕込み量
反応物EpichlorohydrinHCID 7835—
反応物PiperidineHCID 8082—
反応物ethyl 7-hydroxy-4-oxo-4H-chromen-2-carboxylateHCID 5376802—
生成物HCID 21162606HCID 21162606—

反応手順

A mixture of 4.7 g of ethyl 7-hydroxychromone-2-carboxylate and 20 ml of 1-chloro-2,3-epoxypropane is heated at an external temperature of 100° C. for 8 hours in the presence of 0.2 ml of piperidine. The mixture is evaporated under reduced pressure and the residue is taken up with 15 ml of ethyl acetate. After filtration, the solution is evaporated under reduced pressure, the residue is taken up with 30 ml of chloroform and 10 ml of N hydrochloric acid, concentrated and stirred for one hour. The organic layer is washed with water, dried on anhydrous sodium sulfate and evaporated. The residue, crystallized from ethanol, gives 4 g of ethyl 7-(3-chloro-2-hydroxypropoxy)chromone-2-carboxylate. An amount of 1.65 g of the product thus obtained is dissolved in 40 mg of methylene chloride and to the solution thus obtained there is added 0.2 g of hexadecyltributylphosphonium bromide. To the organic solution there is added a solution of CH3SNa in 20 ml of water. The mixture is stirred for two hours at the room temperature, the aqueous layer is separated and acidified with N hydrochloric acid. The precipitate which forms, consisting of 7-(2-hydroxy-3-methylthiopropoxy)chromone2-carboxylic acid, is filtered and dried; m.p. 200°-202° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04282247
出典データセットuspto-grants-1981_08
ORD IDord-281930d7daa0474897d548b88807f102
出典メモuspto-grants-1981_08