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HRID 1019357作成日:2026年10月27日

Methanol → N-Allyl-N,N-di-n-octylamine

https://huagongshe.com/reaction/1019357

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物DioctylamineHCID 3094—
反応物Allyl bromideHCID 7841—
反応物DiisopropylethylamineHCID 81531—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物N-Allyl-N,N-di-n-octylamineHCID 4562804—

反応手順

Vinylsulfomethylpolystyrene resin 3 (0.42 mmol g−1 (est), 160 mg) in DMF (2 cm3) was treated with dioctylamine (1.7 mmol, 515 mm3) at 20° C. for 24 h. The resin was washed with DMF (10×5 cm3) and DCM (10 cm3), resuspended in DMF (2 cm3) and treated with allyl bromide (4.25 mmol, 365 mm3) at 20° C. for 24 h. The solvent and the reagent was then removed by filtration and the resin washed with DCM (2×20 cm3). The elimination was performed in DCM (4 cm3) with DIEA (1.72 mmol, 300 mm3) overnight. The filtrate of this last reaction step was combined with the DCM and MeOH, washed (25 cm3) from the resin and evaporated. It gave 14 contaminated with DIEA in 38 mg yield. The amine was transferred in a little DCM (<5 cm3) to a K2CO3 covered dry silica column (5 g). Impurities were washed away with hexane and the amine eluted with ethyl acetate. After the removal of the solvent 14 was obtained as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06486354B1
出典データセットuspto-grants-2002_11
ORD IDord-16cd478fae0741f69f5e2b4551b2edea
出典メモuspto-grants-2002_11