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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-(1H-pyrrol-1-yl)-1-ethanamine | HCID 2763816 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,2,3,4-Tetrahydropyrrolo(1,2-a)pyrazine | HCID 1549128 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178535B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-e92b5bb6099c469fb05833eb169534f9 |
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| Source note | uspto-grants-2012_05 |
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