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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 402513Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/402513

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-FluorobenzaldehydeHCID 68023—
EduktAminoacetaldehyde dimethyl acetalHCID 89728—
Eduktp-Toluenesulfonic acid monohydrateHCID 521998—
LösungsmittelTolueneHCID 1140—
ProduktN-(2,2-dimethoxyethyl)-N-(4-fluorobenzyl)amineHCID 1161543893,9%

Reaktionsschritte

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+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08742116B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-ac5936983d904b58a6644492d8696f1d
Quellennotizuspto-grants-2014_06