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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 351191생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/351191

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물DioctylamineHCID 3094—
반응물Allyl bromideHCID 7841—
반응물DiisopropylethylamineHCID 81531—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물N-Allyl-N,N-di-n-octylamineHCID 4562804—

반응 단계

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 DIPEA (1.72 mmol, 300 mm3) over night. The filtrate of this last reaction step was combined with the DCM and MeOH wash (25 cm3) from the resin and evaporated. It gave 14 contaminated with DIPEA in 38 mg yield. The amine was transferred in little DCM (<0.5 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 (0.043 mmol, 12 mg, 64%) was obtained as a colourless oil. It was contaminated with 5% of 4 of a previous cycle.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07183367B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-3f9d7d30ba454bcbbaa889d4333c90f2
출처 메모uspto-grants-2007_02