Methanol → HCID 86670057, compound

HRID 1430332Notes

Reaction equation

HRID 1430332 reaction equation
[Cl-].[C:2]([CH2:5][CH2:6][CH2:7][NH+:8]([CH3:10])[CH3:9])([OH:4])=[O:3].S(Cl)([Cl:13])=O.[CH3:15]O>>[Cl-:13].[CH3:15][O:3][C:2](=[O:4])[CH2:5][CH2:6][CH2:7][NH+:8]([CH3:10])[CH3:9]

Participants

4

Conditions

Temperature
45 °C

Procedure

To a solution of 3-carboxy-N,N-dimethyl-1-propanaminium chloride (2) (45.93 g, 0.27 mol) in anh. methanol (300 ml) at −10-0° C. slowly thionyl chloride (55 ml, 0.76 mol) was added and the temperature of the reaction mixture was allowed to rise to ambient temperature during ca. 1 h. The mixture was stirred at 40-50° C. for 3 h and evaporated. The residue was dissolved in acetone (110 ml) and precipitated by adding ether (400 ml). The solid was filtered, washed with ether, and once more dissolved in acetone (110 ml) followed by the precipitation with ether (400 ml). The precipitate was filtered, washed with ether, and dried to give 38.4 g (77%) of 4-methoxy-N,N-dimethyl-4-oxo-1-butanaminium chloride.

Workup

  1. customevaporated
  2. dissolutionThe residue was dissolved in acetone (110 ml)
  3. customprecipitated
  4. additionby adding ether (400 ml)
  5. filtrationThe solid was filtered
  6. washwashed with ether
  7. dissolutiononce more dissolved in acetone (110 ml)
  8. customfollowed by the precipitation with ether (400 ml)
  9. filtrationThe precipitate was filtered
  10. washwashed with ether
  11. customdried

Sources & evidence

ORD record
ord-59d00734a13f483489e1a649702e76e7
Source dataset
uspto-grants-2015_01
Patent number
US08940793B2

Reaction notes

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