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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67804생성일: 2026년 10월 23일

Chloroacetic Acid → Trichlorophenoxyacetic acid

https://huagongshe.com/ko/reaction/67804

반응식

참여 물질

역할이름HCID투입량
반응물Chloroacetic AcidHCID 300—
반응물2,4,5-TrichlorophenolHCID 7271—
반응물2,3,7,8-Tetrachlorodibenzo-P-DioxinHCID 15625—
생성물Trichlorophenoxyacetic acidHCID 1480—

반응 단계

The above objects have been achieved by the synthesis of 2,4,5-trichlorophenoxyacetic acid and its intermediate, 2,4,5-trichlorophenol, which are free from contamination with 2,3,7,8-tetrachloro-dibenzo-p-dioxin (TCDD). The synthesis involves the nitration of 1,2,4-trichlorobenzene to form 1,2,4-trichloro-5-nitrobenzene, which is reduced (usually with hydrogen) to produce 2,4,5-trichloroaniline. The 2,4,5-trichloroaniline is reacted with sulfuric acid and a nitrite to form 2,4,5-trichlorobenzenediazonium sulfate, which is reacted with water and distilled to produce 2,4,5-trichlorophenol which is analytically free of TCDD. The 2,4,5-trichlorophenol is reacted with monochloroacetic acid in the presence of aqueous base, followed by acidification, to produce 2,4,5-trichlorophenoxyacetic acid which also is analytically free of TCDD.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04346248
출처 데이터셋uspto-grants-1982_08
ORD IDord-fba6f8598a6943259c880685fa46ed63
출처 메모uspto-grants-1982_08