HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl 1-methoxycyclopropanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 1-hydroxy-1-cyclopropane carboxylate | HCID 2733178 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 1-methoxycyclopropanecarboxylate | HCID 20393514 | 98.2% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A 0° C. solution of methyl 1-hydroxycyclopropane-1-carboxylate (1 g, 8.61 mmol) in DMF (10 mL) was treated with NaH (60% in mineral oil, 0.689 g, 17.22 mmol), stirred at 0° C. for 0.5 h, treated with iodomethane (0.646 mL, 10.33 mmol), allowed to slowly warm to RT and stirred for 2 h. The mixture was quenched with satd. NH4Cl, diluted with water and extracted with Et2O (3×). The combined organics were washed with water, then brine, dried and concentrated to afford methyl 1-methoxycyclopropane-1-carboxylate (1.10 g, 98%). 1H NMR (400 MHz, DMSO-d6): δ 3.62 (s, 3H), 3.27 (s, 3H), 1.12-1.11 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09309224B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-19bf978b6317485cb332d52f583df81c |
| Source note | uspto-grants-2016_04 |