Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329027Generated: October 30, 2026

Acetyl chloride → N-Benzyl-4-(carbethoxymethoxy)-piperidine

https://huagongshe.com/reaction/329027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant2-((1-Benzylpiperidin-4-yl)oxy)ethanolHCID 20295347—
SolventBenzeneHCID 241—
ProductN-Benzyl-4-(carbethoxymethoxy)-piperidineHCID 2029537366%

Reaction Steps

15.6 g (0.2 mole) of acetyl chloride were added dropwise while cooling at 20° C with an ice bath to a solution of 47 g (0.2 mole) of 2-(1-benzyl-4-piperidyloxy)-ethanol, prepared according to the step B of Example I, and 20.2 g (0.2 mole) of triethylamine in 300 ml of benzene and after standing for 48 hours at room temperature, the precipitate was removed by vacuum filtration. The benzene filtrate was washed with aqueous sodium bicarbonate solution, then water, dried and the benzene distilled off. The residue was distilled to obtain 36.5 g (66% yield) of ethyl 2-(1-benzyl-4-piperidyloxy)-acetate as a clear oil boiling at 160°-170° C at 0.1 mm Hg and having a refractive index nD20 = 1.512.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04018922
Source datasetuspto-grants-1977_04
ORD IDord-a1887121735d4623a5e1f2aebb99ca7d
Source noteuspto-grants-1977_04