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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 483482Erstellt: 25. Oktober 2026

Water → N-(beta-n-butoxyacryloyl)-N-(1-benzyl-4-piperidinyl)aniline

https://huagongshe.com/reaction/483482

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
EduktN-Phenyl-1-(phenylmethyl)-4-piperidinamineHCID 70865—
Edukt3-Butoxyprop-2-enoyl chlorideHCID 53439772—
LösungsmittelDiisopropyl EtherHCID 7914—
ProduktN-(beta-n-butoxyacryloyl)-N-(1-benzyl-4-piperidinyl)anilineHCID 5421063698%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

To a mixture of N-(1-benzyl-4-piperidinyl)aniline (1.8 g), diisopropyl ether (20 ml) and triethylamine (0.87 g) is added dropwise a solution of β-n-butoxyacrylic acid chloride (1.4 g) in diisopropyl ether (5 ml) with stirring and heating at 70° C. After completion of dropwise addition, the mixture is further stirred with heating at the same temperature for 0.5 hour. After cooling, water is added to the reaction mixture and the mixture is subjected to extraction with ethyl acetate. The extract is washed with water and dried over magnesium sulfate. The solvent is distilled off under reduced pressure and the resulting residue is purified by silica gel column chromatography to give N-(β-n-butoxyacryloyl)-N-(1-benzyl-4-piperidinyl)-aniline (2.6 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05225402
Quelldatensatzuspto-grants-1993_07
ORD IDord-961a585b2cfe4d859a4bab81ab32d461
Quellennotizuspto-grants-1993_07