HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Bromo-3-((4-(difluoromethoxy)phenyl)ethynyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-(Difluoromethoxy)-4-iodobenzene | HCID 2737008 | — |
| Reactant | 1-Bromo-3-ethynylbenzene | HCID 11480818 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Bromo-3-((4-(difluoromethoxy)phenyl)ethynyl)benzene | HCID 59790332 | — |
Reaction Steps
To a mixture of 1-bromo-3-ethynylbenzene (9.1 g, 50.26 mmol), TEA (22.38 g, 30.8 mL, 221.1 mmol), PdCl2(ACN)2 (1.41 g, 2.01 mmol) and DMF (60 mL) was added 4-iodo(difluoromethoxy)benzene (10.85 g, 40.21 mmol). The reaction mixture became warm after the addition was completed. The mixture was stirred for 4 h. Then it was poured into water and diluted with EtOAc. The aqueous layer was separated and extracted twice with EtOAc. The combined organic layers were dried over Na2SO4, filtered, and concentrated onto 40 g Celite. Flash chromatography (SiO2, Hexanes) provided 12 g, 92%, of the title compound as a yellow oil that crystallized into a yellow solid upon standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723368B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-92121d58d1d94b39990c9a0300322426 |
| Source note | uspto-grants-2010_05 |