تفاعل #939014

ord-27d7c300e41e40c18111994c03482af2

معادلة التفاعل

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

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe water is slowly removed under vacuum
  2. 2
    أخرىThe solid formed
  3. 3
    ترشيحis filtered off
  4. 4
    workup.ADDITIONafter adding methylene chloride to the batch
  5. 5
    غسيلThe filtrate is washed with water until the aqueous phase
  6. 6
    تجفيفThe organic phase is dried over Na2SO4
  7. 7
    تركيزConcentrating
  8. 8
    أخرىdrying under a high vacuum

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07252791B2uspto-grants-2007_08