Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 18938966 | HCID 18938966 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18938975 | HCID 18938975 | 113.3% |
Reaction Steps
To a solution of 2-(5-methylsulfonylamino-2-methoxyphenyl)-1,3-dioxolane (8.63 g, 31.6 mmol) in DMF (30 ml) was added NaH (1.51 g, 37.9 mmol) and methyl iodide (2.36 ml, 37.9 mmol) and then stirred at 60° C. for 1 hr. After aqueous ammonium chloride was added to the reaction mixture, the mixture was extracted with ether/CH2Cl2. The extract was dried over MgSO4 and evaporated in vacuo to give crude 2-[5-(N-methyl-N-methylsulfonylamino)-2-methoxyphenyl]-1,3-dioxolane (10.29 g) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05837711 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-3a124250e2c0478689e5f7fd4831c581 |
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| Source note | uspto-grants-1998_11 |
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