HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 20770788, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-(4-Trifluoromethylphenyl)benzylchloride | HCID 11459921 | — |
| Reactant | HCID 11984183 | HCID 11984183 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11984464 | HCID 11984464 | — |
| Product | HCID 20770788 | HCID 20770788 | 134,917.297% |
Reaction Steps
Compound 36C (416 mg, 2.0 mmol) was dissolved in acetonitrile (50 mL) with example 36E (568 mg, 2.1 mmol) and Cs2CO3 (1.3 g, 4.0 mmol). The reaction mixture was stirred at RT overnight. Ether (50 mL) and H2O were added and stirring was continued for another 5 min. The layers were separated and the aqueous layer was extracted with ether (2×100 mL). The combined organics was dried over MgSO4 and concentrated to an oil. The crude product was purified by column chromatography eluted with EtOAc and hexanes to give the desired product, compound 36F as a thick yellow oil (597 g, 68%). MS: 443 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06875780B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-1f7ebda563214eacacef74498ab41f8f |
| Source note | uspto-grants-2005_04 |