Reacción #1929061

ord-798bd8c26f824cc794507d9321608b8c

Ecuación de reacción

O=C(Cl)CCl
chloracetylchloride
NCCCCCC(=O)O
6-aminohexanoic acid
Cl
HCl
O=C(O)CCCCCNC(=O)CCl
6-(chloracetamido)hexanoic acid

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe residue was filtered
  2. 2
    LavadoThe residue was then washed with water until the pH of the water
  3. 3
    SecadoThe product, dried over phosphorus pentoxide
  4. 4
    workup.DISSOLUTIONwas re-dissolved in 300 ml chloroform
  5. 5
    Filtraciónfiltered
  6. 6
    Otroto remove the undissolved residue
  7. 7
    workup.ADDITIONHeptane was added to the filtrate
  8. 8
    Otroa syrup was obtained
  9. 9
    workup.STIRRINGby stirring
  10. 10
    Temperaturaunder cooling
  11. 11
    FiltraciónThe product was filtered
  12. 12
    Otrodried
  13. 13
    Otrowas then crystallized from water

Procedimiento

18 mL (221 mMol) chloracetylchloride was added dropwise to 20 g (153 mMol) 6-aminohexanoic acid dissolved in 80 mL cold NaOH solution (2 N) at RT. The reaction mixture was stirred for 30 minutes while the pH of the solution was kept between 10 and 11 with occasional addition of NaOH solution (6 N). The pH of the reaction mixture was then altered to pH 5 with HCl (2 N) and the residue was filtered. The residue was then washed with water until the pH of the water was neutral. The product, dried over phosphorus pentoxide, was re-dissolved in 300 ml chloroform and filtered to remove the undissolved residue. Heptane was added to the filtrate and a syrup was obtained by stirring under cooling. The product was filtered, dried and was then crystallized from water.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08946129B2uspto-grants-2015_02