Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650984Generated: October 30, 2026

Hydrochloric Acid → HCID 15390882, compound

https://huagongshe.com/reaction/650984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantMorpholine, 4-(2-chloroethyl)-, hydrochloride (1:1)HCID 77210—
Reactant2-(3-Phenyl-1,2,4-oxadiazol-5-yl)phenolHCID 779192—
SolventEthanolHCID 702—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 15390882HCID 15390882—

Reaction Conditions

Temperature27.5 °C

Reaction Steps

2.38 g of 5-(2-hydroxyphenyl)-3-phenyl-1,2,4-oxadiazole are dissolved in 100 ml of anhydrous dioxane and stirred with 0.3 g of 80% sodium hydride suspension in oil for 15 minutes at 25-30° C. To this solution is added 75 ml of absolute dioxane, mixed with 3.72 g of 2-(morpholino)ethylchloride hydrochloride and 0.6 g of 80% sodium hydride suspension in oil. This solution is also stirred for 15 minutes at 25-30° C. The combined solutions are heated to 100° C. for 6 hours and then concentrated by evaporation in vacuo. The residue is mixed with water and 20 ml of 1N sodium hydroxide solution and extracted with ethyl acetate. The organic phase is dried over sodium sulphate, the solvent is distilled off in vacuo and the residue is chromatographed on silica gel with ethyl acetate/isopropanol (70:30, mixed with 1.5% of a 25% ammonia solution). The base thus obtained is dissolved in anhydrous ethanol, acidified with ethereal HCl and precipitated with diethyl ether. The residue is recrystallised from anhydrous ethanol and diethylether. Yield: 1.9 g (49% of theory). m.p.: 194-195° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06277872B1
Source datasetuspto-grants-2001_08
ORD IDord-8add4c1e5cec4345a83ead4c55c33e97
Source noteuspto-grants-2001_08