Réaction #1755472

ord-1f61bb4146ab49229678936af8aea13b

Équation de réaction

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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe reaction was quenched with 35 mL water
  2. 2
    Autreto yield
  3. 3
    Autreto provide a clear solution
  4. 4
    ExtractionThe solution was extracted with dichloromethane 2×25 mL
  5. 5
    Séchagedried with Na2SO4
  6. 6
    Autrethe solvent evaporated
  7. 7
    Autreto provide a yellow oil
  8. 8
    Extractionafter extraction

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07989431B2uspto-grants-2011_08