Sodium Lauryl Sulfate → HCID 178443316, compound

HRID 1984958Notes

Reaction equation

HRID 1984958 reaction equation
[Cl-].[CH2:2]([N+:6]1[CH:10]=[CH:9][N:8]([CH3:11])[CH:7]=1)[CH2:3][CH2:4][CH3:5].[S:12]([O-:28])([O:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])(=[O:14])=[O:13].[Na+]>O>[CH2:16]([O:15][S:12]([O-:28])(=[O:14])=[O:13])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27].[CH2:2]([N+:6]1[CH:10]=[CH:9][N:8]([CH3:11])[CH:7]=1)[CH2:3][CH2:4][CH3:5]

Participants

4

Reactant 2

HCID 3423265Sodium Lauryl SulfateHCID 178448538HCID 178448538, compound

Product 1

HCID 178443316HCID 178443316, compoundYield 94.2%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

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.

Workup

  1. customThe water is slowly removed under vacuum
  2. customThe solid formed
  3. filtrationis filtered off
  4. additionafter adding methylene chloride to the batch
  5. washThe filtrate is washed with water until the aqueous phase
  6. dry with materialThe organic phase is dried over Na2SO4
  7. concentrationConcentrating
  8. customdrying under a high vacuum

Sources & evidence

ORD record
ord-5a609bebdbf94d7da30c7ed13c28a698
Source dataset
uspto-grants-2009_06
Patent number
US07544807B2

Reaction notes

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