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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1709035생성일: 2026년 10월 24일

N-Hydroxy-3,4,5-trimethoxybenzamide → 4,4-Diethyl-2-(3,4,5-trimethoxybenzoyl)-3,5-isoxazolidinedione

https://huagongshe.com/ko/reaction/1709035

반응식

참여 물질

역할이름HCID투입량
반응물N-Hydroxy-3,4,5-trimethoxybenzamideHCID 237472—
반응물Diethylmalonyl dichlorideHCID 4149059—
생성물4,4-Diethyl-2-(3,4,5-trimethoxybenzoyl)-3,5-isoxazolidinedioneHCID 13024881.5%

반응 단계

A mixture consisting of 2.27 g (0.0100 mol) of 3,4,5-trimethoxybenzohydroxamic acid (recrystalized from absolute ethanol prior to the reaction), 5 ml of pyridine, and 100 ml of methylene chloride was prepared in a 250 ml round-bottom flask. The mixture was cooled in an ice bath, and 2.00 g (0.0101 mol) of diethylmalonyl chloride was added dropwise over a 15 minute period. The reaction mixture was stirred for one hour at room temperature after which time all of the hydroxamic acid had dissolved. The solution was extracted three times with 50 ml portions of water, four times 50 ml portions of 5% hydrochloric acid, and two times with 50 ml portions of 5% sodium carbonate. The methylene chloride solution was dried (MgSO4) and evaporated to dryness under reduced pressure to give 2.86 g (81.5%) of crude 2-(3,4,5-trimethoxybenzoyl)-4,4-diethylisoxazolidine-3,5-dione as a solid residue: mp 103°-106° C. Recrystallization of 2.72 g of the crude product from 20 ml of absolute ethanol gave 2.14 g of 2-(3,4,5-trimethoxybenzoyl)-4,4-diethylisoxazolidine-3,5-dione: mp 107°-109.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04946963
출처 데이터셋uspto-grants-1990_08
ORD IDord-ba21a5e87ef544b1b29b296638d32358
출처 메모uspto-grants-1990_08