HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dodecanoyl chloride → 4-(N-Dodecanoylaminomethyl)-2-triethylsilylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dodecanoyl chloride | HCID 8166 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Aminomethyl-2-triethylsilylfuran | HCID 15037049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(N-Dodecanoylaminomethyl)-2-triethylsilylfuran | HCID 15037050 | — |
Reaction Steps
Dodecanoyl chloride (109 mg, 0.49 mmol) was added to a solution of 4-aminomethyl-2-triethylsilylfuran (Compound 29, 70 mg, 0.33 mmol) and triethylamine (69 microliter, 0.49 mmol) in tetrahydrofuran (3 ml) at room temperature. After stirring at room temperature overnight (ca. 15 hours), most of the solvent was evaporated and the residue was purified by chromatography on preparative silica thin layer plates (developed with 50% ethyl ether/hexane) to give the title amide as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05037811 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-4ec98eefc3b14565a9c6126e020bd54a |
| Source note | uspto-grants-1991_08 |