HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222285Generated: October 29, 2026
Water → 2-(6-quinolinyloxy)-N-(4-methylpent-2-yn-4-yl) butyramide
https://huagongshe.com/reaction/2222285
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 6-Hydroxyquinoline | HCID 11374 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-bromo-N-(4-methylpent-2-yn-4-yl)butyramide | HCID 21078406 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(6-quinolinyloxy)-N-(4-methylpent-2-yn-4-yl) butyramide | HCID 69253949 | — |
Reaction Steps
6-Hydroxyquinoline (0.46 g) in dry N,N-dimethylformamide (10 ml) was added dropwise to a stirred suspension of sodium hydride (0.10 g, 80% dispersion in mineral oil) in dry N,N-dimethylformamide under an atmosphere of nitrogen at ambient temperature. The green solution was stirred at ambient temperature for 1 hour and a solution of 2-bromo-N-(4-methylpent-2-yn-4-yl) butyramide (0.74 g) in dry N,N-dimethylformamide (10 ml) was added. The mixture was stirred at ambient temperature for 18 hours, poured into water and extracted into diethyl ether (three times). The organic extracts were combined, washed with dilute aqueous sodium hydroxide, water (twice), dried over magnesium sulphate and evaporated under reduced pressure to give a gum. The gum was fractionated by chromatography (silica; diethyl ether) to give the required product, 0.44 g, as a colourless gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07371764B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-e527ddbdcf464a129874042d2677f89f |
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| Source note | uspto-grants-2008_05 |
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