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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019260Generated: October 31, 2026

Triethylamine → HCID 22395371, compound

https://huagongshe.com/reaction/1019260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantButanoic acid, 4-chloro-4-oxo-, ethyl esterHCID 84648—
ReactantPiperonylamineHCID 2723901—
SolventDichloromethaneHCID 6344—
ProductHCID 22395371HCID 2239537133.4%

Reaction Steps

To a solution of 4-piperidone monohydrate hydrochloride (7.68 g, 50 mmol) and triethylamine (21 ml) in methylene chloride (100 ml) was added 3-(ethoxycarbonyl)propionyl chloride (9.87 g, 60 mmol) at 0° C. over a period of 10 min. The mixture was stirred at room temperature for 16 h before being quenched with water (100 ml). The organic layer was separated and the aqueous layer was extracted with methylene chloride (100 ml). The combined organic layers were washed with 1M HCl (100 ml), saturated aqueous sodium bicarbonate (100 ml), and brine (100 ml), dried over sodium sulfate, and concentrated. Purification by flash chromatography (silica gel, 30% ether in hexanes) gave the desired ketone (3.80 g, 33%) as a light yellow oil. 1H NMR (500 MHz, CDCl3) δ1.27 (t, J=7.3 Hz, 3H), 2.48 (t, J=6.4Hz, 2H), 2.53 (t, J=6.4 Hz, 2H), 2.68 (s, 4H), 3.82 (t, J=6.3 Hz, 2H), 3.82 (t, J=6.3 Hz, 2H), 4.16 (q, J=7.3 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486199B1
Source datasetuspto-grants-2002_11
ORD IDord-9e5a40199abd473ab28caf6d925774e1
Source noteuspto-grants-2002_11