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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648538Generated: October 25, 2026

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

https://huagongshe.com/reaction/1648538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantN-Phenyl-1-(phenylmethyl)-4-piperidinamineHCID 70865—
Reactant3-Butoxyprop-2-enoyl chlorideHCID 53439772—
SolventDiisopropyl EtherHCID 7914—
ProductN-(beta-n-butoxyacryloyl)-N-(1-benzyl-4-piperidinyl)anilineHCID 5421063698%

Reaction Conditions

Temperature70 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436254
Source datasetuspto-grants-1995_07
ORD IDord-78e6e2dc8ab54fb691c333e64cf2461f
Source noteuspto-grants-1995_07