HCID 86670058, compound → HCID 51347808, compound

HRID 922098Notes

Reaction equation

HRID 922098 reaction equation
[Br-].[CH2:2]([N+:4]([CH3:13])([CH3:12])[CH2:5][CH2:6][CH2:7][C:8]([O:10]C)=[O:9])[CH3:3]>C(O)C>[CH2:2]([N+:4]([CH3:13])([CH3:12])[CH2:5][CH2:6][CH2:7][C:8]([O-:10])=[O:9])[CH3:3]

Participants

3

Procedure

A solution of N-ethyl-4-methoxy-N,N-dimethyl-4-oxo-1-butanaminium bromide (6a) (6.51 g, 0.025 mol) in ethanol (20 ml) was passed through Amberlite® IRA-410 (OH) ion exchange resin column (190 ml) slowly eluting with ethanol (100 ml). The eluate was evaporated to dryness and the residue was several times azeotropically dried with isopropanol, then dissolved in isopropanol (50 ml) and kept at 0° C. for 12 hours. The mixture was filtered and the filtrate was evaporated. The residue (7.35 g) was mixed with cold ethyl acetate and kept at 0° C. for 12 hours. The mixture was filtered and the precipitate was dried over P2O5 in vacuo to furnish 3.54 g (86%) of 4-[ethyl(dimethyl)ammonio]butanoate. The purity of the material was increased by passing a water solution of 4-[ethyl(dimethyl)ammonio] butanoate through DOWEX® 50WX8 ion exchange resin. The solution was evaporated to dryness; the residue was azeotropically dried with isopropanol followed by drying in vacuo over P2O5 to give 1.27 g (31%) of 4-[ethyl(dimethyl)ammonio]butanoate.

Workup

  1. washslowly eluting with ethanol (100 ml)
  2. customThe eluate was evaporated to dryness
  3. dry with materialazeotropically dried with isopropanol
  4. dissolutiondissolved in isopropanol (50 ml)
  5. filtrationThe mixture was filtered
  6. customthe filtrate was evaporated
  7. additionThe residue (7.35 g) was mixed with cold ethyl acetate
  8. waitkept at 0° C. for 12 hours
  9. filtrationThe mixture was filtered
  10. dry with materialthe precipitate was dried over P2O5 in vacuo

Sources & evidence

ORD record
ord-34dee177e9394ab8800b0aacaf144fc9
Source dataset
uspto-grants-2016_03
Patent number
US09278907B2

Reaction notes

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