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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358975생성일: 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/358975

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 (recrystallized 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 2.86g (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-3,5mp 107- 109.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04999366
출처 데이터셋uspto-grants-1991_03
ORD IDord-3eb402dceb7b48f3af4988e1b58b3a38
출처 메모uspto-grants-1991_03