Reacción #2355145

ord-5c653abacef240c58a2bbc264758f341

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONUpon completion of the addition the reaction mixture
  2. 2
    Otrothe organic layer was separated
  3. 3
    ExtracciónThe aqueous layer was extracted with one 50 mL portion of diethyl ether
  4. 4
    ExtracciónThe combined organic layer and extract
  5. 5
    Lavadowere washed with two 25 mL portions of water
  6. 6
    Secadodried with sodium sulfate
  7. 7
    Filtraciónfiltered
  8. 8
    ConcentraciónThe filtrate was concentrated under reduced pressure

Procedimiento

Under a nitrogen atmosphere, 4.5 mL (0.043 mole) of t-butylamine was added to a solution of 7.7 grams (0.035 mole) of 4-bromobenzoyl chloride in 75 mL of tetrahydrofuran. To this was added dropwise 6.7 mL (0.048 mole) of triethylamine. Upon completion of the addition the reaction mixture was stirred at ambient temperature for about 18 hours, after which it was poured into 50 mL of water, and the organic layer was separated. The aqueous layer was extracted with one 50 mL portion of diethyl ether. The combined organic layer and extract were washed with two 25 mL portions of water, dried with sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure, yielding 8.4 grams of N-t-butyl-4-bromobenzamide, mp 126-128° C. The NMR spectrum was consistent with the proposed structure.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USH0002007H1uspto-grants-2001_12