HuagongsheHuagongshe Chemistry Print Report · For research reference only
12-Methoxydodecanoate → Methyl 12-Methoxydodecanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 12-Methoxydodecanoate | HCID 1420 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetramethylammonium Hydroxide Pentahydrate | HCID 82620 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 12-Methoxydodecanoate | HCID 19611779 | 98.8% |
Reaction Steps
Tetramethylammonium hydroxide pentahydrate (1.7 g, 9.4 mmol) was added to a solution of the title product of Example 1 (2.0 g, 8.7 mmol) in 45 mL of anhydrous acetonitrile. After stirring for 4 hours at room temperature, methyl iodide (0.6 mL, 9.6 mmol) was added and the resulting milky solution stirred at room temperature. The solvent was removed by rotary evaporator and partioned between diethyl ether and water. The organic phase was washed with brine, dried over magnesium sulfate, filtered and concentrated to give the title compound (2.1 g) as a pale yellow liquid. The structure was supported by NMR, infrared spectroscopy, elemental analysis and mass spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05672769 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-afe8575b38b54cf0adfd4f17f0d9b1df |
| Source note | uspto-grants-1997_09 |