HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl 4-cyclobutyl-2-ethyl-5-(imino(methylthio)methyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Methyl 5-carbamothioyl-4-cyclobutyl-2-ethylbenzoate | HCID 86672532 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-cyclobutyl-2-ethyl-5-(imino(methylthio)methyl)benzoate | HCID 68288599 | 114.2% |
Reaction Steps
To a round-bottom flask was added a solution of methyl 5-carbamothioyl-4-cyclobutyl-2-ethylbenzoate (compound 181.6, 1.50 g, 5.41 mmol, 1.00 equiv) in tetrahydrofuran (30 mL). This was followed by the addition of iodomethane (3.80 g, 26.8 mmol, 5.00 equiv) dropwise with stirring. The resulting solution was stiffed at 25° C. for 15 h, then concentrated in vacuo. This resulted in 1.80 g (97%) of the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08871790B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-8f58290a3a984e5cacc93e5bbd7aa69d |
| Source note | uspto-grants-2014_10 |