Réaction #66760

ord-b276a56e587f4d9d87a49145d9afba45

Équation de réaction

O
H2O
COC(=O)c1ccc(B(O)O)cc1
[4-(methoxycarbonyl)phenyl]boronic acid
CCOc1cc(C(=O)OC(C)(C)C)cc(OCC)c1Br
tert-butyl 4-bromo-3,5-diethoxybenzoate
O=P([O-])([O-])[O-].[K+].[K+].[K+]
K3PO4
CCOc1cc(C(=O)OC(C)(C)C)cc(OCC)c1-c1ccc(C(=O)OC)cc1
4-tert-Butyl 4′-methyl 2,6-diethoxybiphenyl-4,4′-dicarboxylate

Solvants

Conditions de réaction

Température
100°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThe reaction mixture was filtered through celite pad
  2. 2
    Concentrationthe filtrate was concentrated under reduced pressure
  3. 3
    AutreThe residue was purified by silicage column chromatography (hexane/EtOAc)
  4. 4
    Autreto give

Mode opératoire

H2O (261 mg, 14.48 mmol) was added to a stirred mixture of PdCl2(dppf) (106 mg, 0.145 mmol), [4-(methoxycarbonyl)phenyl]boronic acid (626 mg, 3.48 mmol), tert-butyl 4-bromo-3,5-diethoxybenzoate (1.00 g, 2.90 mmol) and K3PO4 (1.23 g, 5.79 mmol) in DME (8 ml) and the mixture was stirred at 100° C. overnight. The reaction mixture was filtered through celite pad, the filtrate was concentrated under reduced pressure. The residue was purified by silicage column chromatography (hexane/EtOAc) to give intended compound as a colorless solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08524730B2uspto-grants-2013_09