반응 #939014

ord-27d7c300e41e40c18111994c03482af2

반응 방정식

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
수율 94.2%
CCCCCCCCCCCCOS(=O)(=O)[O-].CCCC[n+]1ccn(C)c1
1-n-Butyl-3-methylimidazolium Lauryl Sulfate
수율 94.2%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The water is slowly removed under vacuum
  2. 2
    기타The solid formed
  3. 3
    여과is filtered off
  4. 4
    workup.ADDITIONafter adding methylene chloride to the batch
  5. 5
    세척The filtrate is washed with water until the aqueous phase
  6. 6
    건조The organic phase is dried over Na2SO4
  7. 7
    농축Concentrating
  8. 8
    기타drying under a high vacuum

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07252791B2uspto-grants-2007_08