Reaktion #1256362

ord-593f292f7dcb438fa12660d7b2657c2a

Reaktionsgleichung

CC(C)(C)[Si](C)(C)OC(=O)C=Cc1ccccc1O[Si](C)(C)C(C)(C)C
3-[2-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acrylic acid tert-butyl-dimethyl-silanyl ester
O=C(Cl)C(=O)Cl
oxalyl chloride
CC(C)(C)[Si](C)(C)Oc1ccccc1C=CC(=O)Cl
3-[2-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-acryloyl chloride

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeat room temperature overnight, the mixture was evaporated to dryness

Vorschrift

To a solution of 10.01 g 3-[2-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acrylic acid tert-butyl-dimethyl-silanyl ester in 25 ml of dichloromethane, three drops of dimethylformamide were added and 4.14 g oxalyl chloride was dropped in at 0° C. After stirring at 0° C. for 90 minutes and then at room temperature overnight, the mixture was evaporated to dryness. The resulting brown solid (7.52 g) was not further purified.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06627763B2uspto-grants-2003_09