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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290887Generated: October 29, 2026

Hydrochloric Acid → HCID 13741757, compound

https://huagongshe.com/reaction/1290887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantAcetonedicarboxylic acidHCID 68328—
Reactant2,5-DimethoxytetrahydrofuranHCID 79098—
Reactant2-MorpholinoethylamineHCID 408285—
SolventWaterHCID 962—
ProductHCID 13741757HCID 13741757—

Reaction Steps

To a solution of 16.2 ml of 2,5-dimethoxytetrahydrofuran in 50 ml of water was added 6 ml of conc. hydrochloric acid. The mixture was stirred at room temperature for 20 minutes. Thereafter, 150 ml of water, 25 ml of 1-(2-aminoethyl)morpholine, 20 ml of conc. hydrochloric acid and 20.1 g of 1,3-acetonedicarboxylic acid were successively added to the reaction mixture. Furthermore, a solution of 8.8 g of Na2HPO4 and 2.5 g of sodium hydroxide in 100 ml of water was added to the mixture. Thereafter the pH was adjusted to the range of 2 to 3. After stirring overnight at room temperature, the reaction solution was washed with chloroform. Potassium carbonate was added to the mixture to render alkaline, followed by extraction with chloroform. The organic layer was washed with water and then dried over anhydrous sodium sulfate. The solvent was then distilled off. The residue was purified by silica gel column chromatography (chloroform:NH3 -saturated methanol=20:1) to give 26.7 g of 8-(2-morpholinoethyl)-8-azabicyclo[3.2.1]octan-3-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753673
Source datasetuspto-grants-1998_05
ORD IDord-45fbed5d83b34f35839bff31dd961b7c
Source noteuspto-grants-1998_05