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HRID 903460作成日:2026年10月26日

Ethyl Acetate → HCID 53771611、化合物

https://huagongshe.com/reaction/903460

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物1,4-DioxaneHCID 31275—
反応物N-HydroxysuccinimideHCID 80170—
反応物4-(4-Chlorophenyl)-2-methyl-4-oxobutanoic acidHCID 2733715—
反応物Potassium ethanethioateHCID 23670855—
溶媒HexaneHCID 8058—
溶媒Water ethanolHCID 19096565—
生成物HCID 53771611HCID 53771611—

反応手順

A solution of 14.3 g. of 3-(4-chlorobenzoyl)-2-methylpropionic acid (Example 47), 7.26 g. of N-hydroxysuccinimide and 13 g. of dicyclohexylcarbidiimide in 150 ml. of dioxane is allowed to stir at room temperature overnight and is then filtered. The filtrate is concentrated at reduced pressure and taken up in 100 ml. of water containing 7.25 g. of L-proline and 10.58 g. of sodium bicarbonate. The mixture is stirred at 25°-35° overnight and filtered through celite. The filtrate is concentrated to remove the ethanol. Concentrated hydrochloric acid is added and the mixture is extracted several times with dichloromethane. The extracts are washed with water and dried (Na2SO4). Evaporation of the solvent yields an amber gum which is dissolved in ethylacetate. Hexane is added, causing white crystals to separate. Recrystallization from ethylacetate gives colorless needles, m.p. 177.5-179.5, labeled isomer A. The preceding compound is brominated as in Example 20 and the product reacted with potassium thioacetate in ethanol-water as in Example 21 to give the product of the Example as a glass.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04226775
出典データセットuspto-grants-1980_10
ORD IDord-a6af1ed9dcfb483ab06f8046dd2fa84e
出典メモuspto-grants-1980_10