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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924007Generated: October 31, 2026

Formaldehyde → 1,2,3,4-Tetrahydropyrrolo(1,2-a)pyrazine

https://huagongshe.com/reaction/1924007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-(1H-pyrrol-1-yl)-1-ethanamineHCID 2763816—
SolventEthanolHCID 702—
Product1,2,3,4-Tetrahydropyrrolo(1,2-a)pyrazineHCID 1549128—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a ethanol solution (20 ml) of 1-(2-aminoethyl)pyrrole (9 mmol) and 37% formaldehyde (9 mmol) was added TFA (0.5 ml) and the resulting reaction mixture was stirred at 50° C. for 15 minutes. It was then cooled to come to 25° C. and stirred at this temperature for 4 hrs. Solvent was removed under reduced pressure, residue was dissolved in ethyl acetate, basified with aqueous sodium carbonate solution, organic layer was separated and dried over sodium sulfate. Evaporation of the organic layer gave the crude 1,2,3,4-Tetrahydro-pyrrolo[1,2-a]pyrazine which was dissolved in dichloromethane (90 ml) at to it DIPEA (12.15 mmol) and boc anhydride (8.9 mmol) were added at 0° C. The resulting reaction mixture was stirred for 16 hrs at 25° C. Organic layer was washed with sodium carbonate, water and brine and finally dried over sodium sulfate. Evaporation of the organic layer gave the crude product which was purified by column chromatography (1% ethyl acetate in dichloromethane). (10% ethyl acetate in hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178535B2
Source datasetuspto-grants-2012_05
ORD IDord-e92b5bb6099c469fb05833eb169534f9
Source noteuspto-grants-2012_05