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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741400Generated: November 1, 2026

Triethylamine → HCID 18367365, compound

https://huagongshe.com/reaction/1741400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl piperidine-2-carboxylateHCID 27517—
Reactant3-Methoxybenzyl chlorideHCID 69994—
SolventDimethylformamideHCID 6228—
ProductHCID 18367365HCID 18367365—

Reaction Steps

A solution of ethyl 2-piperidinecarboxylate (10.0 ml), 3-methoxybenzyl chloride (9.2 ml), and triethylamine (26.6 ml) in N,N-dimethylformamide (64.0 ml) was stirred at room temperature overnight and partitioned between ethyl acetate and water. The organic layer was separated, washed with water (four times) and brine, dried over MgSO4, and evaporated in vacuo. The residue was chromatographed over silica gel to afford ethyl 1-(3-methoxybenzyl)-2-piperidinecarboxylate (12.06 g) as a colorless oil. (+) APCI-MS (m/z): 278 (M+ +1) IR (Film): 1725, 1600, 1260 cm-1NMR (CDCl3, δ): 1.29 (3H, t, J=7.1 Hz), 1.50-1.85 (6H, m), 2.10-2.22 (1H, m), 2.88-3.00 (1H, m), 3.14 (1H, dd, J=6.8, 5.2 Hz), 3.40 (1H, d, J=13.4 Hz), 3.78 (1H, d, J=13.4 Hz), 3.81 (3H, s), 4.21 (2H, q, J=7.1 Hz), 6.77-6.82 (1H, m), 6.89-6.93 (2H, m), 7.17-7.27 (1H, m)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972965
Source datasetuspto-grants-1999_10
ORD IDord-bd55c20eb4b4438f9bf8be2692db29e8
Source noteuspto-grants-1999_10