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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063353Generated: November 1, 2026

Benzylethanolamine → 4-Benzylmorpholine-2-carbonitrile

https://huagongshe.com/reaction/2063353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylethanolamineHCID 4348—
ReactantTetrahydrofuranHCID 8028—
Reactant2-ChloroacrylonitrileHCID 70198—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiethyl EtherHCID 3283—
Product4-Benzylmorpholine-2-carbonitrileHCID 15651195—

Reaction Steps

A mixture of N-benzylethanolamine (intermediate 23, 44.8 ml, 314 mmol) and 2-chloroacrylonitrile (intermediate 24, 25 ml, 314 mmol) was stirred at room temperature for 24 hours. After the mixture was cooled to 0° C., tetrahydrofuran (300 ml)and then potassium tert-butoxide was added to the mixture, and the mixture was stirred at 0° C. for one hour. The mixture was diluted by ethyl ether, and then washed with water and brine and dried over magnesium sulfate. Solvent was removed under reduced pressure, and the residue was purified by silica gel column chromatography (eluent; 5% ethyl acetate in hexane) to afford 4-benzylmorpholine-2-carbonitrile (intermediate 25) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288383B2
Source datasetuspto-grants-2012_10
ORD IDord-1ccc6554106a4e03a7d22a8415e7bde9
Source noteuspto-grants-2012_10