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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503829Generated: November 3, 2026

Benzophenone imine → HCID 59428634, compound

https://huagongshe.com/reaction/503829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenone imineHCID 136809—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 59428624HCID 59428624—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 59428634HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777040B2
Source datasetuspto-grants-2010_08
ORD IDord-71fa03fe975f44df8234f79a4b29b24f
Source noteuspto-grants-2010_08