HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Dimethyl 5-(N-methylmethylsulfonamido)isophthalate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Dimethyl 5-(methylsulfonamido)isophthalate | HCID 3711983 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Dimethyl 5-(N-methylmethylsulfonamido)isophthalate | HCID 11324067 | — |
Reaction Steps
To a stirred suspension of NaH (0.24 g, 10 mmol, 60% in oil dispersion) in 10 mL of DMF was added dimethyl 5-(methylsulfonamido)isophthalate (1.435 g, 5 mmol) followed by iodomethane (0.62 mL, 10 mmol) at room temperature. After 5 h, the reaction was quenched by H2O (25 mL). Then the reaction mixture was extracted with EtOAc, further washed with H2O to remove excess of DMF, dried over anhydrous Na2SO4 and concentrated. The crude product thus obtained was washed with hexanes to give dimethyl 5-(N-methylmethylsulfonamido)isophthalate as a white solid in 91% (1.37 g) yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299267B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-8d7e507390404a2e8d7badc1f9135198 |
| Source note | uspto-grants-2012_10 |