HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 67419815, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 67421220 | HCID 67421220 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 15-Crown-5 | HCID 36336 | — |
| Product | HCID 67419815 | HCID 67419815 | 97% |
Reaction Steps
To a solution of allyl-{2-[4-(4-isopropyl-benzenesulfonylamino)-phenyl]-ethyl}-carbamic acid tert-butyl ester (200 mg, 0.44 mmol) in DMF (5 ml), 15-crown-5, and sodium hydride (20 mg, 0.48 mmol) were added, and the mixture was stirred at room temperature for 30 min. Methyliodide (60 mg, 0.44 mmol) was added and the mixture was stirred for 3 h at room temperature. After concentration in vacuo the residue was partitioned between dichloromethane and saturated aqueous NaHCO3. The organic layer was washed with water, dried over MgSO4, filtered and the solvent evaporated under reduced pressure to give the product as a yellow oil (200 mg, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08232426B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-daa57ec8315142299d4843dcbb6078c8 |
| Source note | uspto-grants-2012_07 |