Reaktion #1755472

ord-1f61bb4146ab49229678936af8aea13b

Reaktionsgleichung

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

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction was quenched with 35 mL water
  2. 2
    Sonstigeto yield
  3. 3
    Sonstigeto provide a clear solution
  4. 4
    ExtraktionThe solution was extracted with dichloromethane 2×25 mL
  5. 5
    Trocknendried with Na2SO4
  6. 6
    Sonstigethe solvent evaporated
  7. 7
    Sonstigeto provide a yellow oil
  8. 8
    Extraktionafter extraction

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07989431B2uspto-grants-2011_08