HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Hydrochloric Acid → Methyl 12-aminododecanoate

HRID 356883
Notes
Print preview

Reaction equation

HRID 356883 reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]([OH:15])=[O:14].Cl.[CH3:17]O>>[NH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]([O:15][CH3:17])=[O:14]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 6966112-Aminododecanoic Acid

Product 1

HCID 3665980Methyl 12-aminododecanoateYield 98%

Procedure

To a suspension of 12-aminododecanoic acid (5.00 g, 23.3 mmol) in anhydrous MeOH (90 mL) was introduced hydrogen chloride gas for 25 minutes, during which time the suspension became clear. The solution was then stirred at room temperature for 3 hours and the solvent was removed in vacuo. The white solid residue was dissolved in H2O. Solid NaHCO3 was added to neutralize the solution to pH 8-9. The white precipitates thus formed were collected by vacuum filtration (5.20 g) (Yield: 98%).

Workup

  • customthe solvent was removed in vacuo
  • dissolutionThe white solid residue was dissolved in H2O
  • additionSolid NaHCO3 was added
  • customThe white precipitates thus
  • customformed
  • filtrationwere collected by vacuum filtration (5.20 g) (Yield: 98%)
  • Sources & evidence

    ORD record
    ord-556f974df338495bab3fc6a50f4c8596
    Source dataset
    uspto-grants-1998_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05840733

    Reaction notes

    Loading…

    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes