Methacrylic Acid → HCID 86733317, compound

HRID 1606566Notes

Reaction equation

HRID 1606566 reaction equation
[C:1]([C:5]1[CH:11]=[C:10]([OH:12])[CH:9]=[C:8]([C:13]([CH3:16])([CH3:15])[CH3:14])[C:6]=1[OH:7])([CH3:4])([CH3:3])[CH3:2].C[CH:18]([C:23]1[CH:29]=C(O)C=C[C:24]=1[OH:25])CC(C)C.[C:31](O)(=O)[CH:32]=C.[C:36](O)(=O)[C:37]([CH3:39])=[CH2:38].FC(F)(F)C(OC(=O)C(F)(F)F)=O.C1(=O)OC(=O)C=C1.FC(F)(F)C(O)=O>>[C:24]([O:12][C:10]1[CH:11]=[C:5]([C:1]([CH3:4])([CH3:3])[CH2:2][C:37]([CH3:39])([CH3:38])[CH3:36])[C:6]([OH:7])=[C:8]([C:13]([CH3:16])([CH3:15])[CH2:14][CH2:31][CH3:32])[CH:9]=1)(=[O:25])[C:23]([CH3:29])=[CH2:18]

Participants

8

Procedure

The compounds of this invention may be prepared according to the method of E. J. Bourne, M. Stacey, J. C. Tetlow, and J. M. Tedder (J. Chem. Soc. 1949 2976) in which one equivalent of a 2,6-di tert.alkyl hydroquinone, such as 2,6-di tert.butyl hydroquinone and 2,6-di tert. 1,3-dimethylbutyl hydroquinone, is reacted with a mixture of 1 to 1.5 equivalents of an α,β-unsaturated organic acid, acrylic acid or methacrylic acid, and 1 to 1.5 equivalents of trifluoroacetic acid anhydride or a mixture of 1 to 1.5 equivalents of an α,β-unsaturated organic acid anhydride such as maleic anhydride and 1 to 1.5 equivalents of trifluoracetic acid. The reaction temperature may vary from room temperature to about 60° C. and the time required to complete the reaction may vary from about 30 minutes to about 12 hours.

Workup

  1. customThe compounds of this invention may be prepared
  2. custommay vary from room temperature to about 60° C.
  3. customthe reaction
  4. waitmay vary from about 30 minutes to about 12 hours

Sources & evidence

ORD record
ord-a54c95ff99c44194a2b0bbfdccfdbb99
Source dataset
uspto-grants-1976_04
Patent number
US03953402

Reaction notes

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