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HRID 1838作成日:2026年10月25日

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

https://huagongshe.com/reaction/1838

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Methylamino)ethanolHCID 8016—
反応物3,4-DichlorobenzaldehydeHCID 22710—
反応物Trimethylsilyl cyanideHCID 82115—
触媒zinc(II)iodideHCID 9883512—
溶媒MethanolHCID 887—
生成物2-(3,4-Dichlorophenyl)-2-[N-(2-hydroxyethyl)-N-methylamino]acetonitrileHCID 19692457—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726313
出典データセットuspto-grants-1998_03
ORD IDord-f2cd038ec84e4a03a81609c6e7029c63
出典メモuspto-grants-1998_03