HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → 2-(5-ethynyl-3-pyridyloxy)-N-(4-methylpent-2-yn-4-yl)butyramide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 2-(5-trimethylsilylethynyl-3-pyridyloxy)-N-(4-methylpent-2-yn-4-yl)butyramide | HCID 21078401 | — |
| Reactant | Diethylether hexane | HCID 21584099 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(5-ethynyl-3-pyridyloxy)-N-(4-methylpent-2-yn-4-yl)butyramide | HCID 21078398 | — |
Reaction Steps
The product from Stage 1 (0.4 g) was dissolved in dichloromethane (10 ml) with stirring and a solution of tetra n-butylammonium fluoride in tetrahydrofuran (1.4 ml, 1M) was added. The mixture was stirred at ambient temperature for 2 hours then stored for 18 hours. Further dichloromethane was added and the organic phase was washed with water (twice), dried over magnesium sulphate and evaporated under reduced pressure to give a gum that was fractionated by chromatography (silica; diethyl ether/hexane, 2:1 by volume) to give the required product, 0.21 g, as a pale brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07166621B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-6ec130d766524b81ba413f0c3c23ed0b |
| Source note | uspto-grants-2007_01 |