HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649026Generated: October 30, 2026
Water → 1H-Pyrrole-3-carboxaldehyde,1-(2-propynyl)-(9CI)
https://huagongshe.com/reaction/649026
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1H-pyrrole-3-carboxaldehyde | HCID 640308 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1H-Pyrrole-3-carboxaldehyde,1-(2-propynyl)-(9CI) | HCID 13604945 | — |
Reaction Steps
2.924 g of pyrrole-3-carboxaldehyde (J. Org. Chem. 1981, Vol. 46, p. 839) dissolved in 45 ml of tetrahydrofuran and 1.488 g of sodium hydride as 50% in oil were admixed and then were stirred for 10 minutes cold, then for 40 minutes at room temperature. After cooling, 2.5 ml of propargyl bromide were added with stirring at 5 C. for 90 minutes. A further 2 ml of propargyl bromide were added with stirring at 5° C. for 1 hour and the mixture was poured into water and extracted with methylene chloride. The solvent was distilled off at atmospheric pressure to obtain 2.868 g of 1-(2-propynyl)-1H-pyrrole-3-carboxaldehyde which was purified by chromatography on silica gel and elution with a 65-35 hexane-ethyl acetate mixture to obtain 2.868 g of the said product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04737513 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-c1e93267b96c4bc2a89d829dc643e1a4 |
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| Source note | uspto-grants-1988_04 |
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