Reacción #2374468

ord-0fae3b3cc7b343b997c59e6b88903d0d

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added dropwise over a 30 minute period
  2. 2
    Temperaturato warm to room temperature
  3. 3
    OtroThe solvent was evaporated
  4. 4
    Otroto give the product in a quantitative yield as a yellow solid

Procedimiento

Under a nitrogen atmosphere, oxalyl chloride (3.8 g, 30 mmol) was combined with methylene chloride (30 mL). The resulting mixture was cooled to 0° C. and dimethylformamide (10 drops) was added. After 5 minutes of stirring a solution of 2-fluoro-α-methyl-biphenylacetic acid (3.0 g, 12 mmol) in methylene chloride (30 mL) was added dropwise over a 30 minute period. The reaction mixture was allowed to warm to room temperature and stirred overnight. The solvent was evaporated to give the product in a quantitative yield as a yellow solid. 1H NMR (CDCl3) δ: 1.58 (d, 3 H), 4.20 (q, 1H), 7.11 (t, 2H), 7.33-7.47 (m, 4H), 7.54 (d, 2H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06083515uspto-grants-2000_07