HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromodifluoroacetate → Ethyl α,α-difluoro-2-quinolineacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Reactant | 2-Bromoquinoline | HCID 2762756 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Ethyl α,α-difluoro-2-quinolineacetate | HCID 10514875 | 70% |
Reaction Steps
2-Bromoquinoline (5.0 g, 24.0 mmol), ethyl 2-bromodifluoroacetate (5.8 g, 28.8 mmol) and copper powder (3.5 g, 55.2 mmol) in DMSO (20 mL) were stirred at 55° C. for 5 hours. The solid was filtered off, water (100 mL) and EA (150 mL) were added. The organic layer was separated, dried over sodium sulfate and concentrated to give the title compound as a yellow oil (4.2 g, 70%), which was used in the next step without further purification. LC-MS (ESI+): m/e 252 (M+H)+, Rt: 0.93 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273068B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-b75998b1f58a4aac89933d1299280816 |
| Source note | uspto-grants-2016_03 |