Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 60136710 | HCID 60136710 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Carbon Dioxide | HCID 280 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 926913-59-9 | HCID 68954028 | 74% |
Reaction Steps
4-Iodo-1,3-dimethyl-5-trifluoromethylpyrazole (8.7 g, 30 mmol) was dissolved in tetrahydrofuran (87 ml), and a solution (1.6 M, 28 ml) of n-butyl lithium in hexane was slowly added under an argon atmosphere with cooling with dryice-acetone (not higher than −60° C.). After stirring at −70° C. for 30 min, the mixture was gradually warmed to room temperature while blowing in carbon dioxide. The reaction mixture was poured into water, the organic layer was removed, and the aqueous layer was acidified with hydrochloric acid. The aqueous layer was extracted with ethyl acetate. The organic layer was washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The obtained crude crystals were washed with hexane to give the desired compound (4.67 g) as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08404861B2 |
|---|
| Source dataset | uspto-grants-2013_03 |
|---|
| ORD ID | ord-beb389f1524247e597fa598a668d66ce |
|---|
| Source note | uspto-grants-2013_03 |
|---|