Reacción #1755472

ord-1f61bb4146ab49229678936af8aea13b

Ecuación de reacción

COc1cc(C=O)ccc1O
Vanillin
COc1cc(C=O)ccc1O
Vanillin
COC(=O)C1CCNCC1
methyl isonipecotate
C#CCBr
propargyl bromide
C#CCN1CCC(C(=O)OC)CC1
1-Prop-2-ynyl-piperidine-4-carboxylic acid methyl ester

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction was quenched with 35 mL water
  2. 2
    Otroto yield
  3. 3
    Otroto provide a clear solution
  4. 4
    ExtracciónThe solution was extracted with dichloromethane 2×25 mL
  5. 5
    Secadodried with Na2SO4
  6. 6
    Otrothe solvent evaporated
  7. 7
    Otroto provide a yellow oil
  8. 8
    Extracciónafter extraction

Procedimiento

To a solution of methyl isonipecotate 3.5 g (24.4 mmol, 3.30 mL) in 100 mL dichloromethane was added TEA (1.5 eq, 36.6 mmol, 5.1 mL), propargyl bromide (3.0 eq, 73.2 mmol, 6.5 ml), at room temperature for 36 hrs. The reaction was quenched with 35 mL water to yield to provide a clear solution. The solution was extracted with dichloromethane 2×25 mL, dried with Na2SO4, and the solvent evaporated to provide a yellow oil. r.f. (40% EtOAc/Hexanes) 0.26 stains faint white with Vanillin, starting material r.f. 0.05 stains yellow with Vanillin. The product appeared pure after extraction.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07989431B2uspto-grants-2011_08