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HRID 28216作成日:2026年10月25日

Water → Ethyl 4-{3-[3-[2-(1-Hydroxycyclohexyl)ethyl]-5,5-dimethyl-4-oxo-2-thiazolidinyl]propyl}benzoate

https://huagongshe.com/reaction/28216

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-Mercapto-2-methylpropanoic acidHCID 78421—
反応物Ethyl 4-(4-oxobutyl)benzoateHCID 12897183—
反応物1-(2-Aminoethyl)cyclohexanolHCID 13371484—
溶媒TolueneHCID 1140—
生成物Ethyl 4-{3-[3-[2-(1-Hydroxycyclohexyl)ethyl]-5,5-dimethyl-4-oxo-2-thiazolidinyl]propyl}benzoateHCID 23339601—

反応手順

A solution of ethyl 4-(4-oxobutyl)benzoate (5.5 g., 0.025 mole) and 1-(2-aminoethyl)cyclohexanol (3.7 g., 0.026 mole) in toluene (40 ml.) is boiled in an open flask for 5 minutes to remove the formed water as the azeotrope. 2-Mercapto-2-methylpropionic acid (3.3 g., 0.0275 mole) is added and the solution is boiled under a Dean-Stark water separator for 5 hours. The solution is then cooled, washed with 2 N hydrochloric acid and water, and dried over sodium sulfate. The solvent is removed at reduced pressure. The residue is chromatographed on 165 g. of silica gel with 2% methanol in chloroform as the eluent. There is obtained 4.6 g. of the title ester as a light yellow, viscous oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04225609
出典データセットuspto-grants-1980_09
ORD IDord-30df19cf7fa14c4bb6861184be4a3131
出典メモuspto-grants-1980_09