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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 402513생성일: 2026년 10월 25일

4-Fluorobenzaldehyde → N-(2,2-dimethoxyethyl)-N-(4-fluorobenzyl)amine

https://huagongshe.com/reaction/402513

반응식

참여 물질

역할이름HCID투입량
반응물4-FluorobenzaldehydeHCID 68023—
반응물Aminoacetaldehyde dimethyl acetalHCID 89728—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
용매TolueneHCID 1140—
생성물N-(2,2-dimethoxyethyl)-N-(4-fluorobenzyl)amineHCID 1161543893.9%

반응 단계

12.4 g of 4-fluorobenzaldehyde were dissolved in 100 mL of toluene and reacted with 10.5 g of 2-aminoacetaldehyde dimethylacetal and 1.90 g of p-toluenesulfonic acid monohydrate for two hours at a Dean Stark apparatus. The solution was allowed to cool down, extracted with saturated sodium bicarbonate solution, water and brine, dried over magnesium sulfate and evaporated to dryness. The crude product was dissolved in 100 mL of ethanol. 1.89 g of sodium borohydride were added portionwise. Stirring was continued overnight. For workup, acetic acid was added until no gas evolution could be observed. Then the solution was evaporated to dryness, taken up in dichloromethane and washed twice with water. The organic layer was extracted with brine, dried over magnesium sulfate and evaporated to dryness. The obtained crude product (20 g) was used for further reactions without purification. Rt=0.86 min (Method B). Detected mass: 182.1 (M-OMe−), 214.2 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08742116B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-ac5936983d904b58a6644492d8696f1d
출처 메모uspto-grants-2014_06