HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Ethyl 1-benzyl-3-methyl-4-oxopiperidine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochloride | HCID 102623 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 1-benzyl-3-methyl-4-oxopiperidine-3-carboxylate | HCID 14666544 | — |
Reaction Steps
Ethyl -1-benzyl-4-oxo-piperidine-3-carboxylate hydrochloride (150 g, 0.504 mol) was suspended in a solvent mixture of 750 ml THF and 750 ml DMF at room temperature. Addition of powdered KOH (56 g, 1.0 mol) was made in two equal lots keeping half an hour interval between two additions. To a clear reaction mixture methyl iodide (78 g, 0.55 mol) was added over period of 10 minutes and it was stirred for three hours at room temperature. The reaction was quenched by adding 4 ltr water followed by 1.5 ltr diethyl ether. Layers were separated. Organic layer was washed with water and dried over Na2SO4. Evaporation of organic solvent afforded a liquid, which was passed through a silica gel column to give 86 g (61%), titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07393957B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-5c09938718774b2a817c6003ab55e3d5 |
| Source note | uspto-grants-2008_07 |