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HRID 231185作成日:2026年10月26日

Ethylenediamine → N-(1-methyl-4-pyrazolylmethyl)trimethylenediamine

https://huagongshe.com/reaction/231185

反応式

関与物質

役割名称HCID仕込み量
反応物EthylenediamineHCID 3301—
反応物AcetonitrileHCID 6342—
反応物1-Methyl-1H-pyrazole-4-carbaldehydeHCID 573117—
生成物N-(1-methyl-4-pyrazolylmethyl)trimethylenediamineHCID 14207161—

反応手順

At room temperature 11 g of 1-methyl-4-pyrazole carbaldehyde was slowly added to 37 g of ethylenediamine in 150 ml of dry acetonitrile. Molecular sieves 4A (a product of Wako Pure Chemicals, Co.) were added as a dehydrating agent to the solution. The mixture was stirred at room temperature for 2 hours, and filtered. Acetonitrile was distilled off under reduced pressure from the filtrate. To the residue was added 100 ml of ethanol, and then 4 g of sodium borohydride was added little by little at room temperature. The mixture was then stirred at room temperature for 2 hours, and ethanol was distilled off under reduced pressure. Water was added to the residue, and the mixture was extracted with dichloromethane. The solvent was distilled off from the dichloromethane layer, and the residue was vacuum-distilled to give 10 g of N-(1-methyl-4-pyrazolylmethyl)trimethylenediamine as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04845106
出典データセットuspto-grants-1989_07
ORD IDord-1c6056e56aa143f5a55368f82175737e
出典メモuspto-grants-1989_07