HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium tert-butoxide → HCID 66638929, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 59799850 | HCID 59799850 | — |
| Reactant | HCID 66639400 | HCID 66639400 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 66638929 | HCID 66638929 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a suspension of (3-ethoxycarbonyl-pyridin-2-ylmethyl)-trimethyl-phosphonium bromide (0.9 g, 2.6 mmol) in 50 mL of ether is added potassium tert-butoxide (0.32 g, 2.9 mmol) and the reaction is heated at reflux for 30 minutes. The reaction is then cooled to −78° C., a solution of (R)-2-dibenzylamino-3-(2-fluoro-phenyl)-propionaldehyde (1.8 g, 3.5 mmol) in 10 mL of ether is added, and the reaction is allowed to stir at room temperature for 16 hours. The reaction is then concentrated under reduced pressure and purification of the resultant residue by silica gel flash column chromatography gives the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08133907B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-93ca0d519ed54805b99dbc8f75466319 |
| Source note | uspto-grants-2012_03 |