Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387978Generated: November 1, 2026

Potassium Phosphate, Tribasic → 8-cyclopropyl-3,4-dihydro-1H-1-benzazepine-2,5-dione

https://huagongshe.com/reaction/2387978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
ReactantCyclopropylboronic acidHCID 2760897—
Reactant8-iodo-2,3,4,5-tetrahydro-1H-1-benzazepine-2,5-dioneHCID 58476623—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product8-cyclopropyl-3,4-dihydro-1H-1-benzazepine-2,5-dioneHCID 6733792323.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 8-iodo-3,4-dihydro-1H-1-benzazepine-2,5-dione (0.6 g, 2.0 mmol) in toluene (9 mL) and H2O (1 mL) under an atmosphere of N2 was added cyclopropylboronic acid (0.34 g, 4.0 mmol), K3PO4 (1.27 g, 6.0 mmol), PCy3 (1.2 mL, 0.8 mmol), and Pd(OAc)2 (90 mg, 0.4 mmol). The reaction mixture was allowed to stir at 80° C. for 12 h and then allowed to cool to rt. To the mixture were added EtOAc (50 mL) and H2O (50 mL), and the resulting solids were filtered over Celite®. The organic solution was separated and the aqueous solution was extracted with EtOAc (2×50 mL). The organic solutions were combined, dried over MgSO4, filtered and concentrated. The residue was purified by column chromatography to provide 8-cyclopropyl-3,4-dihydro-1H-1-benzazepine-2,5-dione (100 mg, 23%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268992B2
Source datasetuspto-grants-2012_09
ORD IDord-d05a269840f94500ae7f419513c8e590
Source noteuspto-grants-2012_09