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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925316Generated: October 31, 2026

Hydrochloric Acid → HCID 67520515, compound

https://huagongshe.com/reaction/1925316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCesium carbonateHCID 10796—
ReactantBenzophenone imineHCID 136809—
ReactantBinap, (A+-)-HCID 634876—
ReactantHCID 86608615HCID 86608615—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67520515HCID 67520515—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 7-(6,7-dimethoxyquinolin-4-yloxy)naphthalen-2-yl trifluoromethanesulfonate (0.825 g, 1.72 mmol) in THF (30 mL), was added Pd(OAc)2 (0.039, 0.17 mmol), followed by BINAP (0.1187 g, 0.19 mmol) and Cs2CO3 (0.784 g, 2.41 mmol). Diphenylmethanimine was added and the mixture was stirred at 65° C. for 16 h. The reaction was cooled to RT, treated with 1N HCl (12 mL) and stirred for 4 h. The mixture was diluted with water and extracted with EtOAc 3×. The aqueous extract was treated with NH4OH until pH=12. This was extracted with EtOAc 3×. The combined organic layers were washed with water and brine, dried over MgSO4, filtered and concentrated in vacuo. The crude material was taken on directly without purification. MS (ESI, pos. ion) m/z: 347.4 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178557B2
Source datasetuspto-grants-2012_05
ORD IDord-bd62f80c0f3948f1a23a4f2d3537dffa
Source noteuspto-grants-2012_05