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O-Xylene → HCID 15376513, compound

HRID 1648192
Notes
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Reaction equation

HRID 1648192 reaction equation
[C:1]1([C:7]2[C:8](=O)[O:9][C:10](C)(C)[O:11][CH:12]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C=[N:17][C:18]([CH3:26])([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[CH3:19].[C:27]1(C)C(C)=CC=CC=1>>[CH3:27][C:8]1[O:9][CH2:10][N:17]([C:18]([CH3:26])([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH3:19])[C:12](=[O:11])[C:7]=1[C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 7237O-XyleneHCID 131570332,2-Dimethyl-5-phenyl-2H,4H-1,3-dioxin-4-oneHCID 15405502HCID 15405502, compound

Product 1

HCID 15376513HCID 15376513, compound

Procedure

Xylene (2 ml) was added to a mixture of 5-phenyl-2,2-dimethyl-2H,4H-1,3-dioxin-4-one (0.82 g) and N-methylene-1-methyl-1-phenylethylamine (0.59 g), and the resulting mixture was heated at reflux for 20 minutes for reaction. The reaction mixture was purified by silica gel chromatography to obtain the captioned compound (0.9 g).

Workup

  1. temperaturethe resulting mixture was heated
temperature
at reflux for 20 minutes for reaction
  • customThe reaction mixture was purified by silica gel chromatography
  • Sources & evidence

    ORD record
    ord-cba4ffcbabdc4382a3078b687bc90027
    Source dataset
    uspto-grants-1995_07
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05436224

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes