Lithium Chloride → HCID 23674028, compound

HRID 411102Notes

Reaction equation

HRID 411102 reaction equation
[C:1]([O-:4])(=[O:3])[CH3:2].[Na+].[CH2:6]([O:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17].[Cl-].[Li+:32]>>[C:1]([O-:4])(=[O:3])[CH3:2].[Li+:32].[CH2:19]([O:18][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30]

Participants

3

Reactant 2

HCID 433294Lithium ChlorideHCID 23713133HCID 23713133, compound2×

Product 1

HCID 23674028HCID 23674028, compound

Procedure

The lauryl ether lithium acetate was prepared by ion-exchanging lauryl ether sodium acetate. Lauryl ether sodium acetate was dissolved in N-butyl alcohol dissolving lithium chloride. The precipitates of sodium chloride, formed by the ion-exchanging reactions, were removed, and N-butyl alcohol in the N-butyl alcohol solution was removed by evaporation under a vacuum, to form lauryl ether lithium acetate.

Workup

  1. customThe precipitates of sodium chloride
  2. customformed by the ion-exchanging reactions
  3. customwere removed
  4. customN-butyl alcohol in the N-butyl alcohol solution was removed by evaporation under a vacuum

Sources & evidence

ORD record
ord-8538a9f65ae6434995e5a74a8d5fce13
Source dataset
uspto-grants-2003_05
Patent number
US06558847B1

Reaction notes

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