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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22476생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/22476

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물DiphosgeneHCID 10426—
반응물2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino)acetic acidHCID 10130412—
용매TetrahydrofuranHCID 8028—
생성물(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetyl chlorideHCID 10198354—

반응 단계

In 30.0 ml of tetrahydrofuran (THF), 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 5.43 g of trichloromethyl chloroformate at 5° C. to a mixture of 80 ml of THF 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 200 ml of ice water to precipitate crystals. The crystals were collected by filtration, washed with 100 ml of ice water, collected by filtration, and then stirred for 30 minutes in 100 ml of n-hexane. After filtration, the resulting crystals were dried under reduced pressure, whereby the title compound was obtained. Yield: 9.2 g (84.3%). Purity: 96.5%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428173
출처 데이터셋uspto-grants-1995_06
ORD IDord-acac927768954aa6bcf8906d5dea0427
출처 메모uspto-grants-1995_06