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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1838생성일: 2026년 10월 23일

2-(Methylamino)ethanol → 2-(3,4-Dichlorophenyl)-2-[N-(2-hydroxyethyl)-N-methylamino]acetonitrile

https://huagongshe.com/ko/reaction/1838

반응식

참여 물질

역할이름HCID투입량
반응물2-(Methylamino)ethanolHCID 8016—
반응물3,4-DichlorobenzaldehydeHCID 22710—
반응물Trimethylsilyl cyanideHCID 82115—
촉매zinc(II)iodideHCID 9883512—
용매MethanolHCID 887—
생성물2-(3,4-Dichlorophenyl)-2-[N-(2-hydroxyethyl)-N-methylamino]acetonitrileHCID 19692457—

반응 단계

A mixture of 10 g of 3,4-dichlorobenzaldehyde and 9.5 ml of cyanotrimethylsilane is cooled in an ice bath, 0.01 g of zinc iodide is added and the mixture is stirred for 15 minutes at RT. A solution of 4.5 g of 2-(methylamino)ethanol in 50 ml of MeOH is then added and the reaction mixture is heated at 60° C. for 2 hours. After one night at RT, it is concentrated under vacuum, the residue is extracted with ether and the organic phase is washed with water, dried over MgSO4 and filtered. The filtrate is acidified to pH 1 by the addition of a saturated solution of hydrochloric acid in ether, acetone is added and the mixture is stirred until crystallization occurs. This gives 15 g of the expected product after wringing of the crystals formed. M.p.=130° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726313
출처 데이터셋uspto-grants-1998_03
ORD IDord-f2cd038ec84e4a03a81609c6e7029c63
출처 메모uspto-grants-1998_03