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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5684생성일: 2026년 10월 24일

Beta-Alanine → 2-Benzylidene-4-methyl-3-oxo-N-phenylpentanamide

https://huagongshe.com/ko/reaction/5684

반응식

참여 물질

역할이름HCID투입량
반응물Beta-AlanineHCID 239—
반응물BenzaldehydeHCID 240—
반응물EthylenediamineHCID 3301—
반응물AnilineHCID 6115—
반응물PiperidineHCID 8082—
반응물Methyl 4-methyl-3-oxopentanoateHCID 2759969—
반응물4-methyl-3-oxo-N-phenylpentanamideHCID 10219899—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매HexaneHCID 8058—
용매HeptaneHCID 8900—
생성물2-Benzylidene-4-methyl-3-oxo-N-phenylpentanamideHCID 53394866—

반응 단계

4-Methyl-3-oxo-N-phenylpentanamide (XIX) is obtained by heating a mixture of methyl 4-methyl-3-oxopentanoate (XX), aniline and ethylene diamine in toluene. 4-Methyl-3-oxo-N-phenylpentanamide (XIX) is subsequently reacted with benzaldehyde in the presence of a catalyst such as, for example, piperidine and glacial acetic acid, ethylene diamine and glacial acetic acid, β-alanine and glacial acetic acid, and the like in an inert solvent such as, for example, toluene, heptane, hexane, and the like for about 24 to about 36 hours at about 60° to about 120° C. with the removal of water to afford 4-methyl-3-oxo-N-phenyl-2-(phenylmethylene)pentanamide (XVIII). Preferably the reaction is carried out with β-alanine and glacial acetic acid at reflux for about 24 hours in hexane. The 4-methyl-3-oxo-N-phenyl-2-(phenylmethylene)pentanamide (XVIII) is reacted with 4-fluorobenzaldehyde in the presence of a catalyst such as, for example, 3-benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chloride, 3,4-dimethyl-5-(2-hydroxyethyl)thiazolium iodide, 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide, thiamine hydrochloride, and the like and a base such as, for example, N,N-diisopropylethylamine, pyridine, N,N-dimethylaniline, triethylamine, 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), 1,4-diazabicyclo[2.2.2]octane (DABCO), 4-dimethylaminopyridine (DMAP), N,N,N',N'-tetramethylethylenediamine (TMEDA) and the like either neat or in the presence of a solvent such as, for example, tetrahydrofuran, tertiary-butyl methyl ether, ethanol, dimethylformamide, dimethylsulfoxide, N-methylpyrrolidone, acetonitrile, methylisobutyl ketone, ethyl acetate, isopropanol, pyridine and the like for about 20 to about 30 hours under anhydrous conditions at about room temperature to about the reflux temperature of the solvent to afford the compound of Formula XVII. Preferably the reaction is carried out in the presence of 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide and the triethylamine in ethanol at about 75°-80° C. for about 24 hours. The compound of Formula XVII is reacted with a compound of Formula ##STR45## wherein R10 and R11 are alkyl of one to either carbon atoms or R10 and R11 together are ##STR46## --CH2CH2 --or --CH2CH2CH2 --in the presence of a catalyst of Formula

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245047
출처 데이터셋uspto-grants-1993_09
ORD IDord-030dd67a47da476ca971ca42ed1f5543
출처 메모uspto-grants-1993_09