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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2231270생성일: 2026년 10월 25일

Toluene → N-(2-(2,4,6-Trichlorophenoxy)ethyl)-1-propanamine

https://huagongshe.com/reaction/2231270

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물(Dimethyl sulfide)trihydroboronHCID 12423031—
반응물N-(n-propyl)-2,4,6-trichlorophenoxyacetamideHCID 13488356—
용매MethanolHCID 887—
생성물N-(2-(2,4,6-Trichlorophenoxy)ethyl)-1-propanamineHCID 3842173—

반응 조건

온도60 °C

반응 단계

N-(n-propyl)-2,4,6-trichlorophenoxyacetamide, 44.0 gm, was added to 250 ml of toluene. 28 ml of borane methyl sulfide [BH3.(CH3)2S] (2 equivalents) was then slowly added to the system. The system was heated at approximately 60° C. for 15 hours at which time reaction completion was checked by IR spectroscopy. 200 ml of methanol was then slowly added to the system. After addition of the methanol, the system was acidified by bubbling in HCl gas. Afterwards, the system was refluxed for 1 hour. The solvent was then removed by stripping. The resulting oil was dissolved in methanol which was then stripped. The oil was next dissolved in methylene chloride. The organic solution was washed with a sodium hydroxide solution and then with water. The methylene chloride was removed by stripping to give 36.3 gm of the N-(n-propyl)ethanolamine 2,4,6-trichlorophenylether, as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04782074
출처 데이터셋uspto-grants-1988_11
ORD IDord-4d43b419ab554148bfee1976e0a9f5c5
출처 메모uspto-grants-1988_11