HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252963Generated: October 31, 2026
Ethanolamine → 1-(2-Hydroxyethyl)-2,5-dimethylpyrrole
https://huagongshe.com/reaction/2252963
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Pivalic acid | HCID 6417 | — |
| Reactant | 2,5-Hexanedione | HCID 8035 | — |
| Reactant | Heptane | HCID 8900 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Hydroxyethyl)-2,5-dimethylpyrrole | HCID 95963 | — |
Reaction Steps
A mixture of hexan-2,5-dione (5 g), ethanol amine (26.7 g) and pivalic acid (23.26 g) in a solvent mixture containing n-heptane: tetrahydrofliran: toluene (4:1:1, 50 mL) was refluxed with stirring at 110-120° C. Water formed during the reaction was removed azeotropically during 3 to 4 hrs. The reaction mixture was cooled and the solvent was removed. The residue obtained was dissolved in dichloromethane (30 mL), washed with saturated sodium bicarbonate solution (30 mL), water (30 mL), and then with brine (30 mL), dried (Na2SO4) and the solvent was evaporated. The crude compound obtained as an oily mass, was purified by column chromatography (silica gel 100-200), using ethyl acetate:hexane (2:8) as an eluent to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07323491B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-e2a83902dbf645bebd5aa023a6ccea25 |
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| Source note | uspto-grants-2008_01 |
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