HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Dibromo-1,2,2,2-tetrafluoroethane → Tert-butyl 5,6-dibromo-2,4-difluoronicotinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Dibromo-1,2,2,2-tetrafluoroethane | HCID 168688 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Tert-butyl 5-bromo-2,4-difluoronicotinate | HCID 71281815 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 5,6-dibromo-2,4-difluoronicotinate | HCID 89421760 | 77% |
Reaction Steps
Into a solution of TMPMgCl LiCl (1.0 M×6.8 mL, 6.8 mmol) in THF (5.0 mL) at −45° C. was added dropwise a solution of tert-butyl 5-bromo-2,4-difluoronicotinate (1.32 g, 4.5 mmol) in THF (5.0 mL). The mixture was stirred for 15 min then dibromotetrafluoroethane (1.0 mL, 6.8 mmol) was added. After 15 min at −45° C., the temperature was allowed to rise to room temperature. The reaction was quenched with saturated NH4Cl and extracted with ethyl acetate. The organic layers were combined, dried over sodium sulfate and evaporated. The residue was purified by silica chromatography (0-10% ethyl acetate in hexanes) to give tert-butyl 5,6-dibromo-2,4-difluoronicotinate (1.29 g, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409905B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-b073b292df5e4ac4910db82692fd7ec1 |
| Source note | uspto-grants-2016_08 |