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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641032Generated: November 2, 2026

Chloroacetonitrile → HCID 57266187, compound

https://huagongshe.com/reaction/1641032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantTriethylamineHCID 8471—
Reactant4-PiperidineethanolHCID 73953—
SolventDiethyl EtherHCID 3283—
ProductHCID 57266187HCID 57266187100%

Reaction Steps

The title compound was prepared according to general procedure G described in Scheme 3. 2-(Piperidin-4-yl)ethanol (1.2 g, 9.3 mmol) was treated with 2-chloroacetonitrile (1.4 g, 18.6 mmol), triethylamine (10.4 mL, 74.3 mmol) and stirred at RT for 14 h. The crude reaction mixture was diluted with Et2O (25 mL) and washed with H2O (3×10 mL). The organic layer was dried over Na2SO4 and concentrated under reduced pressure to afford the title compound as a yellow oil (1.56 g, 100%), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114894B2
Source datasetuspto-grants-2012_02
ORD IDord-adf550375f0241da9941e8ecd8a40cf2
Source noteuspto-grants-2012_02