HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzophenone imine → HCID 59428634, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzophenone imine | HCID 136809 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 59428624 | HCID 59428624 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59428634 | HCID 59428634 | — |
Reaction Steps
A 25-mL round-bottomed flask equipped with magnetic stirrer and reflux condenser is charged with rac-2,2′-bis(diphenylphosphino)-1,1′-binapthyl (0.040 g, 0.063 mmol), Pd2dba3 (0.019 g, 0.021 mmol) and sodium tert-butoxide (0.282 g, 2.94 mmol). The reaction vessel is then purged with a stream of nitrogen for 0.5 h. After such time, a solution of Compound 1b (0.600 g, 2.10 mmol) in toluene (6 mL) followed by benzophenone imine (0.45 g, 2.51 mmol) is added. The reaction is then heated at reflux for 2 h. After such time the reaction is cooled to room temperature and concentrated under reduced pressure. The resulting oil is then purified by column chromatography to afford Compound 1c as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07777040B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-71fa03fe975f44df8234f79a4b29b24f |
| Source note | uspto-grants-2010_08 |