HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13268818, compound → HCID 13268828, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13268818 | HCID 13268818 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13268828 | HCID 13268828 | 99.5% |
Reaction Conditions
| Temperature | -20 °C |
|---|
Reaction Steps
A solution of 21.2 g (80.0 mmol) of 2-(pentafluorophenyl)-4,4-dimethyl-2-oxazoline (Bull. Chem. Soc. Jpn., 57, 225 (1984)) in 300 ml of dry ether was cooled to -20° C. under argon and treated with 60 ml of 1.6M methyl lithium (96.0 mmol). The solution was stirred at -20° C. for two hours, then stirred at room temperature overnight. The mixture was diluted with water, and the organic layer was dried over magnesium sulfate and concentrated to give 20.8 g of the title compound as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04920120 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-ab88cebcc141499b9b9e560a831e2bf9 |
| Source note | uspto-grants-1990_04 |