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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920554Generated: October 29, 2026

Benzophenone imine → HCID 86670013, compound

https://huagongshe.com/reaction/920554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenone imineHCID 136809—
ReactantSodium BicarbonateHCID 516892—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
Reactant4-Benzyl-2-(4-bromo-phenyl)-morpholineHCID 58097879—
SolventTolueneHCID 1140—
ProductHCID 86670013HCID 8667001363.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a degassed solution of 4-benzyl-6-(4-bromo-phenyl)-morpholine (4.00 g; 12.04 mmol) in toluene (50 mL) was added benzophenone imine (2.42 mL; 14.45 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.60 g; 0.96 mmol), tris-(dibenzylideneacetone)-dipalladium(0) (0.22 g; 0.24 mmol) and NaOtBu (1.62 g; 16.86 mmol). The resulting mixture was heated to 100° C. for 16 hours. After cooling to RT a 5% aqueous NaHCO3 solution was added, and the product was extracted with EtOAc. The combined organic layers were dried (Na2SO4), filtered, and concentrated in vacuo. The residue was purified by column chromatography (SiO2, Et2O:hexanes 1:1) to afford benzhydrylidene-[4-(4-benzyl-morpholin-2-yl)-phenyl]-amine (3.30 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273017B2
Source datasetuspto-grants-2016_03
ORD IDord-07e21d9cbd0849e5a2446532b66c8c3f
Source noteuspto-grants-2016_03