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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413774Generated: November 2, 2026

Triethylamine → HCID 23045638, compound

https://huagongshe.com/reaction/2413774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantButyryl chlorideHCID 8855—
Reactant1-(3-Methoxyphenyl)piperidineHCID 605725—
ReactantTriethylazanium chlorideHCID 12698378—
SolventTolueneHCID 1140—
ProductHCID 23045638HCID 23045638—

Reaction Steps

Butyryl chloride (2.0 g, 0.019 mol) in dry toluene (5 ml) was slowly added to a solution of 3-methoxyphenylpiperidine (2.45 g, 0.013 mol) and triethylamine (1.92 g, 0.013 mol) in dry toluene at 5°. The mixture was stirred at room temperature for 30 min., whereupon the triethylammonium chloride formed was filtered off and the solvent evaporated. The crude N-butyryl-3-(3-methoxyphenyl)piperidine (2.82 g) dissolved in dry tetrahydrofuran (30 ml) was added to a suspension of LiAlH4 (2.0 g) in dry tetrahydrofuran (30 ml) under nitrogen. After reflux for 3 h the mixture was hydrolysed, the precipitate filtered off and the solvent evaporated. The residue dissolved in light petroleum was passed through an alumina column. (Alternatively the residue could be distilled in vacuo.) The product was precipitated as the hydrochloride and recrystallized from ethanol/ether yielding the pure product (3.6 g, 88%) mp 130°-1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04719219
Source datasetuspto-grants-1988_01
ORD IDord-704a6a690c27431f91ff8d73d2dc80d0
Source noteuspto-grants-1988_01