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

HCID 69859806, compound → HCID 23508311, compound

HRID 1883714
Notes
Print preview

Reaction equation

HRID 1883714 reaction equation
[C:1]([NH:4][C:5]1[CH:6]=[CH:7][C:8]([C:14]([CH3:21])=[CH:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[C:9]2[C:13]=1[CH2:12][CH2:11][CH2:10]2)(=[O:3])[CH3:2]>C(O)C.[Pd]>[C:1]([NH:4][C:5]1[CH:6]=[CH:7][C:8]([CH:14]([CH3:21])[CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[C:9]2[C:13]=1[CH2:12][CH2:11][CH2:10]2)(=[O:3])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 69859806HCID 69859806, compound

Product 1

HCID 23508311HCID 23508311, compoundYield 86.8%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 702EthanolSolvent

Procedure

A solution of ethyl 3-[7-acetylamino-indan-4-yl]-but-2-enoate (1.9 g, Reference Example 7) in ethanol (200 mL) was hydrogenated over 10% palladium on charcoal for 16 hours. The mixture was filtered through diatomaceous earth and the filtrate was evaporated to give the title compound (1.66 g).

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  • filtrationThe mixture was filtered through diatomaceous earth
  • customthe filtrate was evaporated
  • Sources & evidence

    ORD record
    ord-434ee3510dec4a728e8def25a85bbf26
    Source dataset
    uspto-grants-2004_07
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US06762199B2

    Reaction notes

    Loading…