反応 #1755472

ord-1f61bb4146ab49229678936af8aea13b

反応方程式

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

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The reaction was quenched with 35 mL water
  2. 2
    その他to yield
  3. 3
    その他to provide a clear solution
  4. 4
    抽出The solution was extracted with dichloromethane 2×25 mL
  5. 5
    乾燥dried with Na2SO4
  6. 6
    その他the solvent evaporated
  7. 7
    その他to provide a yellow oil
  8. 8
    抽出after extraction

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07989431B2uspto-grants-2011_08