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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 903460생성일: 2026년 10월 26일

Ethyl Acetate → HCID 53771611, 화합물

https://huagongshe.com/reaction/903460

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물1,4-DioxaneHCID 31275—
반응물N-HydroxysuccinimideHCID 80170—
반응물4-(4-Chlorophenyl)-2-methyl-4-oxobutanoic acidHCID 2733715—
반응물Potassium ethanethioateHCID 23670855—
용매HexaneHCID 8058—
용매Water ethanolHCID 19096565—
생성물HCID 53771611HCID 53771611—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04226775
출처 데이터셋uspto-grants-1980_10
ORD IDord-a6af1ed9dcfb483ab06f8046dd2fa84e
출처 메모uspto-grants-1980_10