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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22472생성일: 2026년 10월 24일

Dimethylformamide → (2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetyl chloride

https://huagongshe.com/ko/reaction/22472

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Phosphorus oxychlorideHCID 24813—
반응물2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino)acetic acidHCID 10130412—
용매1,2-DimethoxyethaneHCID 8071—
생성물(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetyl chlorideHCID 10198354—

반응 단계

In 50.0 ml of 1,2-dimethoxyethane (DME), 10.0 g of 2- (5-amino-1,2,4-thiadiazol-3-yl)-2(Z)-methoxyiminoacetic acid were stirred at -20° C., followed by the dropwise addition of a chlorinating reagent, which had been prepared beforehand by gradually adding 8.4 g of phosphorus oxychloride at 5° C. to a mixture of 20 ml of DME and 4.0 g of N,N-dimethylformamide (DMF) and then reacting them for 30 minutes. After they were reacted for 5 minutes, the reaction mixture was poured into 160 ml of ice water to precipitate crystals. The resulting crystals were collected by filtration, washed with 200 ml of ice water and then stirred for 30 minutes in 120 ml of n-hexane. After filtration, the resulting crystals were dried under reduced pressure, whereby the title compound was obtained. Yield: 8.43 g (76.6%). Purity: 97.2%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428173
출처 데이터셋uspto-grants-1995_06
ORD IDord-0757c3bbfa1d443bb6f3447a86ec152b
출처 메모uspto-grants-1995_06