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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174244Generated: October 30, 2026

Ethylurea → HCID 89650197, compound

https://huagongshe.com/reaction/2174244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylureaHCID 12254—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 89650598HCID 89650598—
SolventAcetonitrileHCID 6342—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 89650197HCID 8965019720.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

Compound ii (1.0 g, 3.7 mmol) and N-ethylurea (362 mg, 4.1 mmol) were dissolved in degassed dioxane (50 mL) under an atmosphere of argon. Potassium tert-butoxide (628 mg, 5.6 mmol), Xantphos (129 mg, 0.22 mmol) and palladium(0)bis(dibenzylideneacetone) (65 mg, 0.11 mmol) were added sequentially. The mixture was heated at 100° C. with stirring under argon for 16 h. Additional palladium(0)bis(dibenzylideneacetone) (65 mg, 0.11 mmol) and N-ethylurea (560 mg, 6.4 mmol) were added and the mixture heated at reflux for 5 h. The mixture was cooled to RT, diluted with acetonitrile (100 mL) and then adsorbed on to silica by concentration in vacuo. The crude product was purified by flash chromatography (40 g GraceResolv silica cartridge, 0-10% MeOH in EtOAc) to afford iii as a light brown solid (244 mg, 20%). [M+H]+ m/z=320.05.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09060515B2
Source datasetuspto-grants-2015_06
ORD IDord-f7f33f2c5bf54a988560868ae88d1d67
Source noteuspto-grants-2015_06