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Dimethylformamide dimethyl acetal → HCID 21939863, compound

HRID 1242900
Notes
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Reaction equation

HRID 1242900 reaction equation
CO[CH:3](OC)[N:4]([CH3:6])[CH3:5].[C:9]([NH:12][C:13]1[CH:14]=[C:15]2[C:19](=[CH:20][CH:21]=1)[C:18](=[O:22])[CH2:17][CH2:16]2)(=[O:11])[CH3:10]>>[CH3:3][N:4](/[CH:6]=[C:17]1/[C:18](=[O:22])[C:19]2[C:15]([CH2:16]/1)=[CH:14][C:13]([NH:12][C:9](=[O:11])[CH3:10])=[CH:21][CH:20]=2)[CH3:5]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 78373Dimethylformamide dimethyl acetalHCID 312894N1-(1-oxo-2,3-dihydro-1H-inden-5-yl)acetamide

Product 1

HCID 21939863HCID 21939863, compound

Conditions

Temperature
100 °C

Procedure

Dimethylformamide dimethylacetal was added to 5-acetamido-1-indanone (2.5 g, 13.2 mmol), which was stirred at 100° C. for 3.5 hours, and cooled to room temperature. The precipitated crude products were collected, which was washed with ethyl acetate to give the titled compound (2.73 g).

Workup

  1. temperaturecooled to room temperature
  2. customThe precipitated crude products
  3. customwere collected
On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes
  • washwhich was washed with ethyl acetate
  • Sources & evidence

    ORD record
    ord-8e459ffcea8549cabb7946ba3da3ae7f
    Source dataset
    uspto-grants-2006_10
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07115750B1

    Reaction notes

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