反应 #1956799

ord-2a634375f9704b8780ed0dc778dac0f6

反应方程式

CCCCOP(=O)(OCCCC)OCCCC
Tributylphosphate
Cn1ccnc1
N-methylimidazole
CCCCOP(=O)([O-])OCCCC.CCCC[N+]1(C)C=CN=C1
product
收率 98.3%
CCCCOP(=O)([O-])OCCCC.CCCC[N+]1(C)C=CN=C1
N-methyl-N-butylimidazolium dibutylphosphate
收率 98.3%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGThe liquid was stirred at the same temperature for an additional 5 hours
  2. 2
    温度The liquid was cooled
  3. 3
    其他moved to a rotary evaporator
  4. 4
    其他dried at 150° C./5 mm Hg for 4 hours

实验过程

Tributylphosphate (137.2 g, 0.505 mole) was added dropwise, slowly, to a 300 ml flask containing 41.5 g (99%, 0.5 mole) N-methylimidazole at 170° C. under nitrogen and stirring. The liquid was stirred at the same temperature for an additional 5 hours. The liquid was cooled and moved to a rotary evaporator and dried at 150° C./5 mm Hg for 4 hours. The product (171.3 g, yield 98%) was pure, as judged from NMR, and was liquid at room temperature. 1H-NMR (CDCl3, 300.13 MHz, δ): 10.37 (s, 1H, —N—CH═N—), 7.50 (s, 1H, —N—CH═CH—N—), 7.29)s, 1H, —N—CH═CH—N—), 4.09 (t, 2H, —N—CH2—CH2CH2CH3), 3.87 (s, 3H, —N—CH3), 3.67 (m, 4H, —O—CH2—CH2CH2CH3), 1.67 (qu, 2H, —NCH2—CH2—CH2CH3), 1.40 (m, 4H, 2×—OCH2—CH2—CH2CH3), 1.16 (m, 4H, —OCH2CH2—CH2—CH3), 1.16 (m, 2H, —NCH2CH2—CH2CH3), 0.70 (m, 6H, 2×—OCH2CH2CH2—CH3), 0.70 (m, 3H, —NCH2CH2CH2—CH3). 31P-NMR (CDCl3, 81.015 MHz, δ): 0.95 [s, (RO)2—P(═O)—O−].

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07638636B2uspto-grants-2009_12