HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexachloroethane → Tert-butyl 5-chloro-2,4-difluoronicotinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexachloroethane | HCID 6214 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Tert-butyl 2,4-difluoronicotinate | HCID 71281946 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 5-chloro-2,4-difluoronicotinate | HCID 71281897 | 48.1% |
Reaction Steps
Into a solution of LDA in THF (20 mL, 12 mmol) was added a solution of tert-butyl 2,4-difluoronicotinate (2.14 g, 10 mmol) in THF (12 mL) at −78° C. The mixture was stirred for 30 min and then a solution of hexachloroethane (2.96 g, 12.5 mmol) in THF (7.0 mL) was added. The temperature was allowed to rise to 0° C. The reaction was then quenched with saturated NH4Cl. The mixture was extracted with ethyl acetate and the organic layers were combined, dried over sodium sulfate, evaporated and purified by silica chromatography (0-8% ethyl acetate in hexanes) to give tert-butyl 5-chloro-2,4-difluoronicotinate (1.2 g, 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409905B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-88a20d163dd5466797e222ab737558cc |
| Source note | uspto-grants-2016_08 |