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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896176Generated: November 1, 2026

2-Chloroethyl chloroformate → 2-(5-Phenyl-1,2,4-oxadiazol-3-yl)morpholine hydrochloride

https://huagongshe.com/reaction/1896176

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroethyl chloroformateHCID 12305—
Reactant4-Benzyl-2-(5-phenyl-1,2,4-oxadiazol-3-yl)morpholineHCID 58097882—
Solvent1,2-DichloroethaneHCID 11—
Product2-(5-Phenyl-1,2,4-oxadiazol-3-yl)morpholine hydrochlorideHCID 66842498—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred solution of 4-benzyl-2-(5-phenyl-1,2,4-oxadiazol-3-yl)morpholine (intermediate 27, 900 mg, 2.80 mmol) in 1,2-dichloroethane (2.0 ml) was added chloroethyl chloroformate (0.46 ml, 4.20 mmol), and the reaction mixture was stirred at 70° C. for 4 hours. The reaction mixture was concentrated in vacuo. After removal of the solvent, the residue was dissolved in methanol (2.0 ml), and the solution was stirred under reflux for one hour. When the reaction was complete (checked by thin layer chromatography), the reaction mixture was concentrated in vacuo. The resulting 2-(5-phenyl-[1,2,4]oxadiazol-3-yl)-morpholine hydrochloride (intermediate 28) was used for next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518939B2
Source datasetuspto-grants-2013_08
ORD IDord-f12cdea224d1460d9fa98a09d1e847d5
Source noteuspto-grants-2013_08