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HRID 471115作成日:2026年10月27日

p-Toluenesulfonic acid → Ethyl 2-cyclopropylthiazole-4-carboxylate

https://huagongshe.com/reaction/471115

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Ethyl 2-(cyclopropanecarboxamido)-3-mercaptopropanoateHCID 57989028—
溶媒TolueneHCID 1140—
生成物Ethyl 2-cyclopropylthiazole-4-carboxylateHCID 18771956—

反応手順

A solution of ethyl 2-(cyclopropanecarboxamido)-3-mercaptopropanoate (example 57, step a) (5 g) and tosic acid (0.875 g) in toluene (100 mL) was heated at reflux under Dean and Stark conditions overnight. The reaction was allowed to cool and the toluene solution was washed with saturated sodium hydrogen carbonate solution (3×100 mL) dried over sodium sulphate, filtered and evaporated. The resulting brown gum was redissolved in acetonitrile (100 mL). Manganese dioxide (40 g) was added and the mixture heated at reflux overnight. The reaction was filtered through Celite and the filter pad washed with MeCN (3×100 mL). The combined filtrate and washings were evaporated and the residue purified by silica gel chromatography eluting with 9:1 to 4:1 isohexane:ethyl acetate gradient. The fractions containing product were combined and evaporated to give the subtitled compound as a clear oil. Yield 0.15 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08629271B2
出典データセットuspto-grants-2014_01
ORD IDord-20edbe6bf1e447d69b3e3d47fb3f047f
出典メモuspto-grants-2014_01