反应 #1755473

ord-fc93313ee4ed4c0e85b286462542df1b

反应方程式

C#CCBr
propargyl bromide
CC(C)(C)OC(=O)N1CCNCC1
tert-butyl-1-piperazine carboxylate
C#CCBr
propargyl bromide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
C#CCN1CCN(C(=O)OC(C)(C)C)CC1
yellow oil
收率 46.0%
C#CCN1CCN(C(=O)OC(C)(C)C)CC1
4-Prop-2-ynyl-piperazine-1-carboxylic acid tert-butyl ester
收率 46.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The residue was evaporated to dryness
  2. 2
    workup.ADDITIONDichloromethane, 50 mL, and water, 50 mL, were added
  3. 3
    萃取The reaction mixture was extracted with CH2Cl2, 4×40 mL
  4. 4
    干燥dried over magnesium sulfate
  5. 5
    其他evaporate
  6. 6
    其他to provide a brown oil
  7. 7
    其他purify with a RT Scientific system

实验过程

To a solution of 10.0 g (54.8 mmol) of tert-butyl-1-piperazine carboxylate in 60 mL acetonitile was added 5.20 mL (60.4 mmol) propargyl bromide and 37.9 g (274 mmol) anhydrous potassium carbonate. Additional propargyl bromide, 1.5 mL, was added after stirring for 36 hours at room temperature. The residue was evaporated to dryness. Dichloromethane, 50 mL, and water, 50 mL, were added. The reaction mixture was extracted with CH2Cl2, 4×40 mL, dried over magnesium sulfate, and evaporate to provide a brown oil. The oil was dissolved in dichloromethane and purify with a RT Scientific system using hexane/ethyl acetate gradient to yield 5.5 g (46%) of yellow oil, which ultimately crystallized upon standing.

来源

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