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HRID 402513作成日:2026年10月25日

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

https://huagongshe.com/reaction/402513

反応式

関与物質

役割名称HCID仕込み量
反応物4-FluorobenzaldehydeHCID 68023—
反応物Aminoacetaldehyde dimethyl acetalHCID 89728—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒TolueneHCID 1140—
生成物N-(2,2-dimethoxyethyl)-N-(4-fluorobenzyl)amineHCID 1161543893.9%

反応手順

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+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08742116B2
出典データセットuspto-grants-2014_06
ORD IDord-ac5936983d904b58a6644492d8696f1d
出典メモuspto-grants-2014_06