HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 58265699, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(4-Bromo-3-chlorophenyl)acetamide | HCID 2746295 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58265699 | HCID 58265699 | — |
Reaction Steps
To a solution of 4-bromo-3-chloroacetanilide (10.0 g, 40.2 mmol) in 50 mL THF is added 60% sodium hydride in mineral oil (2.40 g, 60.0 mmol) and the reaction mixture is stirred for 1 h at RT. The reaction mixture is cooled to 0° C., methyliodide (2.49 mL, 40.0 mmol) is added. After 2 h additional methyl iodide (0.25 mL, 4.0 mmol) is added and the reaction mixture is stirred at RT for 10 min. The reaction mixture is quenched with saturated aqueous ammonium chloride, filtered and extracted with diethyl ether. The organic phases are washed with brine, dried over Na2SO4 and evaporated to dryness. Yield: 10.3 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304556B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-81812a8da37240fcbe1a04f9cf70e2a2 |
| Source note | uspto-grants-2012_11 |