HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 23039700, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Trimethylsulfonium iodide | HCID 75127 | — |
| Reactant | 1-[2-Chloro-4-(4-chlorophenoxy)phenyl]ethan-1-one | HCID 677479 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23039700 | HCID 23039700 | — |
Reaction Steps
DMSO (150 mL) was added dropwise to a mixture of sodium hydride (22 g) in THF (600 mL). After completion of the addition a solution of trimethylsulfonium iodide (171 g) in DMSO (300 mL) was added slowly at 5° C. whereupon a solution of 1-[2-chloro-4-(4-chlorophenoxy)phenyl]ethanone (107 g) in DMSO (300 mL) was added carefully. The mixture was stirred for 1 h at room temperature and dil. NH4Cl solution was added. The mixture was extracted with MTBE (3×) and the combined organic phases were washed with water, dried and evaporated to obtain the desired compound that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09247746B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-b37ba3fbf1c34340a361306fe0dd4206 |
| Source note | uspto-grants-2016_02 |