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

Hydrogen chloride-ethyl acetate → HCID 68430454, compound

HRID 2191288
Notes
Print preview

Reaction equation

HRID 2191288 reaction equation
[CH3:1][C@H:2]([O:5][C:6]1[CH:7]=[CH:8][C:9]2[CH2:10][N:11](C(OC(C)(C)C)=O)[CH2:12][CH2:13][O:14][C:15]=2[N:16]=1)[CH2:3][CH3:4].[ClH:24].C(OCC)(=O)C>>[ClH:24].[CH3:1][C@H:2]([O:5][C:6]1[CH:7]=[CH:8][C:9]2[CH2:10][NH:11][CH2:12][CH2:13][O:14][C:15]=2[N:16]=1)[CH2:3][CH3:4]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 21866389Hydrogen chloride-ethyl acetateHCID 68430280HCID 68430280, compound

Product 1

HCID 68430454HCID 68430454, compoundYield 70%

Procedure

A mixture of the compound obtained in step 1 (0.70 g) and 4N hydrogen chloride/ethyl acetate (5 mL) was stirred at room temperature for 3 hr. The precipitate was collected by filtration, and the aqueous layer was basified and extracted with ethyl acetate and aqueous sodium hydroxide solution. The organic layer was washed with saturated brine and dried, and the solvent was evaporated under reduced pressure. Ethyl acetate was added to the residue, and 4N hydrogen chloride/ethyl acetate was added. The precipitate was collected by filtration, and recrystallized from ethanol-diisopropyl ether to give the title compound (0.40 g, 70%) as a white powder.

Workup

  1. filtrationThe precipitate was collected by filtration
  • extractionextracted with ethyl acetate and aqueous sodium hydroxide solution
  • washThe organic layer was washed with saturated brine
  • customdried
  • customthe solvent was evaporated under reduced pressure
  • additionEthyl acetate was added to the residue, and 4N hydrogen chloride/ethyl acetate
  • additionwas added
  • filtrationThe precipitate was collected by filtration
  • customrecrystallized from ethanol-diisopropyl ether
  • Sources & evidence

    ORD record
    ord-4150ea8f5d3249e28373dd60ed6b8419
    Source dataset
    uspto-grants-2012_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08329687B2

    Reaction notes

    Loading…

    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes