HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 21890139, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | o-Xylyl bromide | HCID 6992 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 21890637 | HCID 21890637 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21890139 | HCID 21890139 | 45% |
Reaction Steps
Acetonitrile (10 ml) was added to the compound (1) (139 mg), 2-methylbenzyl bromide (0.03 ml), and potassium carbonate (81 mg), and the mixture was stirred at room temperature overnight. Water was added to the reaction solution, and the mixture was extracted with chloroform. The extract was washed with saturated brine and was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by thin-layer chromatography using chloroform/methanol for development. Diethyl ether was added to the purification product, and the precipitated crystal was collected by filtration and was washed to give the title compound (46 mg, yield 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135466B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-11763085a1fe449a9a61e85d3aa1e0ec |
| Source note | uspto-grants-2006_11 |