HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741621Generated: October 28, 2026
2-Methyl-3-butyn-2-ol → HCID 86748033, compound
https://huagongshe.com/reaction/1741621
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methyl-3-butyn-2-ol | HCID 8258 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 13250604 | HCID 13250604 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 86748033 | HCID 86748033 | — |
Reaction Steps
A stirred mixture of 12.6 g of 5-bromo-2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)nicotinic acid, methyl ester, 3.4 g of 3-hydroxy-3-methyl-1-butyne, 0.02 g of bis(triphenylphosphine)palladium(II)-chloride, 0.04 g of triphenylphosphine, and 0.02 g of cuprous iodide in 300 mL of dry triethylamine is heated at reflux for 72 hours. The reaction is then filtered hot through celite, and the filtering agent is washed with methylene chloride. The combined filtrates were concentrated in vacuo, and the residue is partitioned between dilute aqueous hydrochloric acid and methylene chloride. The organic phase is washed with brine, dried, concentrated in vacuo, and the residue is chromatographed on silica gel using ether-methylene chloride mixtures to afford the desired product, mp 142°-145°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05334576 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-8f94773bd9ee4ce5acf33fa238654dc7 |
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| Source note | uspto-grants-1994_08 |
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