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HRID 509156Erstellt: 26. Oktober 2026

Potassium Phosphate, Tribasic → 2-(2,4,6-Trimethylphenyl)-3-methoxy-cyclopent-2-enone

https://huagongshe.com/reaction/509156

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt2,4,6-Trimethylbenzeneboronic acidHCID 292184—
Edukt2-Bromo-3-methoxycyclopent-2-enoneHCID 11095426—
Katalysatorpalladium(II) acetateHCID 167845—
Katalysator2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
LösungsmittelTolueneHCID 1140—
Produkt2-(2,4,6-Trimethylphenyl)-3-methoxy-cyclopent-2-enoneHCID 1557764676,3%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a suspension of 2-bromo-3-methoxy-cyclopent-2-enone (6.75 g, 35.3 mmol), 2,4,6-trimethylphenyl boronic acid (6.99 g, 42.6 mmol) and freshly ground potassium phosphate (15 g, 70.6 mmol) in degassed toluene (180 ml) under nitrogen are added Pd(OAc)2 (159 mg, 0.71 mmol) and S-Phos (579 mg, 1.41 mmol), and the reaction heated to 90° C. with stirring under N2 for 4 hours. The reaction mixture is partitioned between ethyl acetate (150 ml) and water (150 ml), and the organic layer is removed, Silica gel is added to the organic layer, the solvent is evaporated under reduced pressure and the residue is purified by flash chromatography on silica gel to give 2-(2,4,6-trimethylphenyl)-3-methoxy-cyclopent-2-enone (6.2 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09096560B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-322cfeffc88d47a0b5314d424c032dea
Quellennotizuspto-grants-2015_08