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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2259433생성일: 2026년 10월 27일

Allylamine → N-(3-phenylallyl)-allylamine

https://huagongshe.com/reaction/2259433

반응식

참여 물질

역할이름HCID투입량
반응물AllylamineHCID 7853—
반응물TriethylamineHCID 8471—
반응물Benzene, (3-chloro-1-propenyl)-HCID 94242—
용매TetrahydrofuranHCID 8028—
생성물N-(3-phenylallyl)-allylamineHCID 471790733.1%

반응 조건

온도60 °C

반응 단계

175 ml (1.27 mol) of triethylamine were added to 173 ml (1.16 mol) of cinnamyl chloride in 1,350 ml of tetrahydrofuran, the mixture was heated to 60° C., and then 105 ml (1.40 mol) of allylamine were added dropwise. The mixture was refluxed for 6 h and then stirred at room temperature for 10 h. After concentration under water pump vacuum, the contents of the flask were partitioned between methyl t-butyl ether and water (pH=10). The aqueous phase was extracted twice more with methyl t-butyl ether and subsequently the combined organic phases were extracted with a mixture of 250 ml of concentrated hydrochloric acid and 2 l of water. The aqueous phase was then extracted with 1.2 l of methylene chloride, and the methylene chloride phase washed five times with 500 ml of 10% strength hydrochloric acid each time. The combined aqueous phases were made alkaline with concentrated sodium hydroxide solution and extracted twice with methylene chloride. Drying and concentration of the organic phase resulted in 66.5 g of crude product which was distilled at 86°-88° C. under oil pump vacuum (0.25 mbar). Yield: 64 g (32%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05473080
출처 데이터셋uspto-grants-1995_12
ORD IDord-415a2796422a4af4aa11d8764c00e038
출처 메모uspto-grants-1995_12