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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461724Generated: November 3, 2026

Triethylamine → HCID 14851351, compound

https://huagongshe.com/reaction/1461724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAzacyclonolHCID 15723—
Reactant3-Methoxybenzyl chlorideHCID 69994—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14851351HCID 14851351102.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 8.0 g (30 mmol) of α,α-diphenyl-4-piperidinomethanol, 2.35 g (15 mmol) of 3-methoxybenzyl chloride, 0.5 g of triethylamine and 30 ml of THF is stirred under reflux for 1 hour, during which a colorless precipitate separates out. After cooling to 20° C., the precipitate is filtered off, and the filtrate is concentrated. For working up, the residue is taken up in 5 ml of methylene chloride, and ethereal HCl solution is added until no further precipitation occurs. The mixture is diluted with 30 ml of methylene chloride, the precipitate is filtered, and the filtrate is concentrated. Drying of the oily residue at 40° C. in vacuo results in 6.5 g of final product. Decomposition point about 80° C. Characteristic IR bands: 3360, 1590, 1480, 1438, 1256, 690 cm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05077301
Source datasetuspto-grants-1991_12
ORD IDord-8c3b903e8ed64d9ab6549ed108c9bed6
Source noteuspto-grants-1991_12