HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 3772327, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 1-(3-Chloro-5-trifluoromethyl-pyridin-2-yl)-ethanone | HCID 21712136 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 3772327 | HCID 3772327 | 98% |
Reaction Steps
608 mg of a sodium ethoxide 21% ethanol solution was added at 0° C. to a tetrahydrofuran (dehydrated) 9 mL solution of 1 g of 2-acetyl-3-chloro-5-(trifluoromethyl)pyridine and 635 mg of ethyl 2,2,2-trifluoroacetate, followed by stirring at room temperature for 13 hours. After completion of the reaction, water was added to the reaction liquid, followed by extraction with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain 1.4 g of 1-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)-4,4,4-trifluorobutan-1,3-dione (after-mentioned intermediate No. IX-25).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124760B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-79ad4b602d2a42eeb48367943b2540fb |
| Source note | uspto-grants-2012_02 |