HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Chloro-6-(trifluoroacetoacetyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Dibenzo-18-crown-6 | HCID 26541 | — |
| Reactant | 1-(6-Chloropyridin-2-yl)ethanone | HCID 11579167 | — |
| Catalyst | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-6-(trifluoroacetoacetyl)pyridine | HCID 11601268 | — |
Reaction Steps
To a mixture of ethyl trifluoroacetate (17.2 g) and sodium hydride (60% in oil, 5.7 g) in THF (200 ml) is added a solution of 1A (11.2 g) in THF (50 ml) with ethanol (2 drops) and a solution of dibenzo-18-crown-6 (415 mg) in THF (70 ml). The reaction mixture is stirred for 60 h at ambient temperature. After heating for 1 h at reflux temperature, the mixture is acidified with 2M hydrochloric acid and extracted with ethyl acetate. The organic phase is dried and evaporated. One obtains the crude title compound as an oily product (21.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06528456B2 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-d3c2dbb0fcf7488bbcacf0dcf21a7e67 |
| Source note | uspto-grants-2003_03 |