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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287855Generated: November 2, 2026

Hydrochloric Acid → HCID 21506798, compound

https://huagongshe.com/reaction/1287855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl SulfateHCID 6163—
Reactant2,3-Dihydro-4H-spiro[naphthalene-1,3'-piperidine]-2',4,6'-trioneHCID 17928—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
ProductHCID 21506798HCID 21506798128.8%

Reaction Steps

To 24.3 grams (0.1 M) of 2,3-dihydrospiro-[naphthalene-1(4H),3'-piperidine]-2',4,6'-trione in 300 milliliters of dry dimethylformamide maintained under nitrogen atmosphere was added with stirring 4.37 grams (0.1 M) of a 55 per cent suspension of sodium hydride in mineral oil. After stirring for five minutes, 16.0 grams (0.1 M) of diethyl sulfate were added in one portion. The slightly exothermic reaction mixture was allowed to stir for a short time and concentrated hydrochloric acid was added dropwise until the reaction mixture was slightly acidic. The reaction solvent was removed under reduced pressure at steam bath temperature and the resulting oil extracted into ether. The ether extracts were washed with 5 percent sodium hydroxide solution, water, and then dried (MgSO4). After filtration, the ether was removed, leaving a residue, which was recrystallized from diethyl ether to give 34.9 grams (64%) of 1'-ethyl-2,3-dihydrospiro-[naphthalene-1(4H),3'-piperidine]-2',4,6'-trione, melting point 85.5°-89° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03985888
Source datasetuspto-grants-1976_10
ORD IDord-9270429a0ab54c6992aa61be44f0ebcd
Source noteuspto-grants-1976_10