HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl (4-oxo-4,10-dihydro-9-oxa-3-thiabenzo[f]azulen-6-ylsulfanyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | (4-Oxo-4,10-dihydro-9-oxa-3-thiabenzo[f]azulen-6-ylsulfanyl)acetic acid | HCID 68488427 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl (4-oxo-4,10-dihydro-9-oxa-3-thiabenzo[f]azulen-6-ylsulfanyl)acetate | HCID 86649442 | 88.1% |
Reaction Steps
Methyl iodide (6.5 mL, 104 mmol) and potassium hydrogencarbonate (17.0 g, 170 mmol) were added to a DMF (200 mL) solution of the compound obtained in Example 21 (26.1 g, 85 mmol), and the mixture was stirred at room temperature overnight. The solvents were distilled off under a reduced pressure, water was added to the residue, and the product was extracted with ethyl acetate. The organic layer was washed with a saturated sodium chloride solution and then dried over anhydrous sodium sulfate, and the solvents were distilled off under a reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1), to give 24.0 g (88%) of the captioned compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377967B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-9da0e7f55a5e4a94b37ee17d1e2aa756 |
| Source note | uspto-grants-2013_02 |