反应 #939014

ord-27d7c300e41e40c18111994c03482af2

反应方程式

CCCC[n+]1ccn(C)c1.[Cl-]
1-n-butyl-3-methylimidazolium chloride
CCCCCCCCCCCCOS(=O)(=O)[O-].[Na+]
sodium lauryl sulfate
CCCCCCCCCCCCOS(=O)(=O)[O-].CCCC[n+]1ccn(C)c1
product
收率 94.2%
CCCCCCCCCCCCOS(=O)(=O)[O-].CCCC[n+]1ccn(C)c1
1-n-Butyl-3-methylimidazolium Lauryl Sulfate
收率 94.2%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The water is slowly removed under vacuum
  2. 2
    其他The solid formed
  3. 3
    过滤is filtered off
  4. 4
    workup.ADDITIONafter adding methylene chloride to the batch
  5. 5
    洗涤The filtrate is washed with water until the aqueous phase
  6. 6
    干燥The organic phase is dried over Na2SO4
  7. 7
    浓缩Concentrating
  8. 8
    其他drying under a high vacuum

实验过程

15.30 g (87.6 mmole) of 1-n-butyl-3-methylimidazolium chloride (BMIM Cl) and 26.60 g (minimum 87.6 mmole) of sodium lauryl sulfate (technical grade, content 95-99%) are dissolved in 50 ml of hot water. The water is slowly removed under vacuum. The solid formed is filtered off after adding methylene chloride to the batch. The filtrate is washed with water until the aqueous phase is colourless and free from chloride. The organic phase is dried over Na2SO4. Concentrating and drying under a high vacuum gives 33.40 g of product (82.5 mmole; 94% of the theoretical yield, based on BMIM Cl) which is obtained as a white beige waxy solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07252791B2uspto-grants-2007_08