HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl 1-(diphenylmethyl)azetidine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Diphenylmethyl)azetidine-3-carboxylic acid | HCID 2735440 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 1-(diphenylmethyl)azetidine-3-carboxylate | HCID 2759842 | 80.8% |
Reaction Steps
A solution of 1-benzhydrylazetidine-3-carboxylic acid (4.20 g) in N,N-dimethylformamide (45 ml) were added potassium carbonate (6.53 g) and iodomethane (0.976 ml), followed by stirring at room temperature for 20.5 hr. The reaction mixture was poured into ice water, and extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate. The solvent was removed, and the residue was purified by silica gel column chromatography (eluent; heptane:ethyl acetate=5:1, then 3:1). Fractions containing the target compound were concentrated to provide the titled compound as yellow crystals (3.57 g, 80.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07855290B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-e92459fe410f4f0f8ad8d80559c16fde |
| Source note | uspto-grants-2010_12 |