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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029821Generated: October 27, 2026

Hydrochloric Acid → 1-(4-Methoxy-5,6,7,8-tetrahydro-1-naphthyl)-2-ethyl-3-pyrrolidino-1-propanone

https://huagongshe.com/reaction/1029821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantPyrrolidine, hydrochloride (1:1)HCID 212848—
Reactant1-(4-Methoxy-5,6,7,8-tetrahydro-1-naphthyl)-1-butanoneHCID 14994236—
SolventIsopropanolHCID 3776—
Product1-(4-Methoxy-5,6,7,8-tetrahydro-1-naphthyl)-2-ethyl-3-pyrrolidino-1-propanoneHCID 1407133462.8%

Reaction Steps

A mixture of 1-(4-methoxy-5,6,7,8-tetrahydro-1-naphthyl)-1-butanone (2.50 g), paraformaldehyde (0.42 g), pyrrolidine hydrochloride (1.51 g), and hydrochloric acid (0.2 ml) in isopropyl alcohol (7 ml) was refluxed for 15 hours. The reaction mixture was evaporated in vacuo to give the residue. The residue was partitioned into water and ethyl ether. The aqueous layer, was extracted, neutralized with ammonia water, and then extracted with ethyl ether. The organic layer was dried over anhydrous magnesium sulfate. The mixture was filtered and the filtrate was evaporated in vacuo to give 1-(4-methoxy-5,6,7,8-tetrahydro-1-naphthyl)-2-ethyl-3-pyrrolidino-1-propanone (2.13 g, Yield: 62.8%) as an oil. ##STR186##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05103022
Source datasetuspto-grants-1992_04
ORD IDord-fda365c92be948c78a4d721f8c24ce8f
Source noteuspto-grants-1992_04