反应 #543590

ord-c6b3e33fc2f54b9e84d96ba6e171a089

反应方程式

CCCCC(C(=O)O)C(=O)O
n-butylmalonic acid
C1CCNCC1
piperidine
C=O
formaldehyde
C=C(CCCC)C(=O)O
title compound
收率 97.5%
C=C(CCCC)C(=O)O
2-Butyl acrylic acid
收率 97.5%

溶剂

反应条件

温度
80°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.DISSOLUTIONgradually redissolved over 1 hour
  2. 2
    温度then cooled to room temperature
  3. 3
    其他The solvents were removed under reduced pressure
  4. 4
    workup.DISSOLUTIONthe residue was dissolved in ethyl acetate (200 ml)
  5. 5
    洗涤washed successively with 1 M hydrochloric acid and brine
  6. 6
    干燥dried over anhydrous magnesium sulfate
  7. 7
    过滤filtered
  8. 8
    浓缩The filtrate was concentrated

实验过程

To a solution of n-butylmalonic acid (17.2 g, 107 mmol) in ethanol (200 ml) was added piperidine (12.76 ml, 129 mmol) and 37% aq. formaldehyde (40.3 ml, 538 mmol). The solution was heated to 80° C. during which time a precipitate appeared and gradually redissolved over 1 hour. The reaction mixture was stirred at 80° C. overnight then cooled to room temperature. The solvents were removed under reduced pressure and the residue was dissolved in ethyl acetate (200 ml), washed successively with 1 M hydrochloric acid and brine, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated to give the title compound as a clear oil (13.37 g, 97%). 1H-NMR; δ (CDCl3), 6.29 (1H, s), 5.65 (1H, s), 2.34–2.28 (2H, m), 1.54–1.26 (4H, M), 0.94 (3H, t, J=7.1 Hz).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07186719B2uspto-grants-2007_03