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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7440Generated: October 25, 2026

Hydrochloric Acid → Edonerpic

https://huagongshe.com/reaction/7440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant3-Hydroxyazetidine hydrochlorideHCID 2759290—
Reactant5-[2-(3-Chloropropyloxy)ethyl]benzo[b]thiopheneHCID 21990069—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductEdonerpicHCID 990194664.2%

Reaction Conditions

Temperature65 °C

Reaction Steps

In 30 mL of dimethyl sulfoxide was dissolved 6.50 g of 5-[2-(3-chloropropoxy)ethyl]-1-benzothiophene, and to the solution were added 5.60 g of 3-azetidinol hydrochloride and 15.3 mL of a 5.mol/L aqueous sodium hydroxide solution, after which the resulting mixture was stirred at 65° C. for 3.5 hours. After the reaction mixture was cooled, water and ethyl acetate were added thereto and the pH was adjusted to 1 with 6 mol/L hydrochloric acid, and the aqueous layer was separated. Ethyl acetate was added to the aqueous layer and the pH was adjusted to 10 with a 5 mol/L aqueous sodium hydroxide solution, after which the organic layer was separated. The organic layer was washed with water and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The residue was purified by a column chromatography (eluent; chloroform:methanol=30:1 to 10:1) to obtain 4.77 g of 1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087594B2
Source datasetuspto-grants-2006_08
ORD IDord-ecef0c41657b40eb8c5d05201a090f57
Source noteuspto-grants-2006_08