Reacción #691384

ord-406e1e4503ff4a0baef6094958b54c76

Ecuación de reacción

c1ccncc1
pyridine
CC(=O)Cl
acetyl chloride
COC(=O)CCCCCN.Cl
6-Aminohexanoic acid methyl ester hydrochloride
Cl
hydrochloric acid
COC(=O)CCCCCNC(C)=O
methyl 6-acetylamino-hexanoate

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe mixture is separated
  2. 2
    Lavadothe organic layer is washed with a saturated brine
  3. 3
    Secadodried over magnesium sulfate
  4. 4
    Concentraciónconcentrated under reduced pressure

Procedimiento

6-Aminohexanoic acid methyl ester hydrochloride (5 g) is dissolved in methylene chloride (20 ml) and thereto are added pyridine (4.5 ml) and acetyl chloride (2 ml), and the mixture is stirred at room temperature for 1 hour and 45 minutes. To the reaction solution are added a 1N-hydrochloric acid and chloroform, and the mixture is separated, and the organic layer is washed with a saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give methyl 6-acetylamino-hexanoate (5.19 g) as a crude product. MS (m/z): 188 [M+H]+

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07906517B2uspto-grants-2011_03