Reaktion #170870

ord-ca1bcf550773409ab01884f95d98b7ed

Reaktionsgleichung

FC1(F)Oc2ccc(Br)cc2O1
5-bromo-2,2-difluoro-benzo[1,3]dioxole
CC#N
acetonitrile
CCN(CC)CC
triethylamine
COC(=O)c1ccc2c(c1)OC(F)(F)O2
2,2-difluoro-benzo[1,3]dioxole-5-carboxylic acid methyl ester

Lösungsmittel

Reaktionsbedingungen

Temperatur
75°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe cooled reaction mixture
  2. 2
    Filtrationwas filtered
  3. 3
    Sonstigethe filtrate was evaporated to dryness
  4. 4
    SonstigeThe residue was purified by silica gel column chromatography

Vorschrift

A solution of 5-bromo-2,2-difluoro-benzo[1,3]dioxole (11.8 g, 50.0 mmol) and tetrakis(triphenylphosphine)palladium (0) [Pd(PPh3)4, 5.78 g, 5.00 mmol] in methanol (20 mL) containing acetonitrile (30 mL) and triethylamine (10 mL) was stirred under a carbon monoxide atmosphere (55 PSI) at 75° C. (oil bath temperature) for 15 hours. The cooled reaction mixture was filtered and the filtrate was evaporated to dryness. The residue was purified by silica gel column chromatography to give crude 2,2-difluoro-benzo[1,3]dioxole-5-carboxylic acid methyl ester (11.5 g), which was used directly in the next step.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08846753B2uspto-grants-2014_09