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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266773Generated: October 26, 2026

Diisopropyl Ether → N-(beta-ethoxyacryloyl)-N-(1-benzyl-4-piperidinyl)aniline

https://huagongshe.com/reaction/266773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl EtherHCID 7914—
ReactantN-Phenyl-1-(phenylmethyl)-4-piperidinamineHCID 70865—
Reactant3-Ethoxy-2-propenoyl chlorideHCID 3014429—
SolventTriethylamineHCID 8471—
ProductN-(beta-ethoxyacryloyl)-N-(1-benzyl-4-piperidinyl)anilineHCID 5419452189.3%

Reaction Steps

To a mixture of N-(1-benzyl-4-piperidinyl)aniline (0.9 g), diisopropyl ether (30 ml) and triethylamine (0.5 g) is added β-ethoxyacrylic acid chloride (0.7 g) in portions at 60° C. After refluxing for 1 hour, the reaction mixture is poured into ice-water and extracted with ethyl acetate. The extract is dried and concentrated and to the resulting residue is added n-hexane and the formed crystals are separated by filtration and recrystallized from n-hexane to give N-(β-ethoxyacryloyl)-N-(1-benzyl-4-piperidinyl)aniline (1.1 g) as white powders, m.p. 106°-108° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652247
Source datasetuspto-grants-1997_07
ORD IDord-74d6a48fc34d420ea124ea78ca355e48
Source noteuspto-grants-1997_07