Isobornylmethacrylate → HCID 131718422, compound

HRID 1109081Notes

Reaction equation

HRID 1109081 reaction equation
[CH3:1][C:2]([C:4]([O:6][CH:7]1[C@@:12]2([CH3:16])[C:13]([CH3:15])([CH3:14])[C@H:9]([CH2:10][CH2:11]2)[CH2:8]1)=[O:5])=[CH2:3]>C(OCC)(=O)C>[CH3:3][C:2]([C:4]([O:6][CH:7]1[C@@:12]2([CH3:16])[C:13]([CH3:15])([CH3:14])[C@H:9]([CH2:10][CH2:11]2)[CH2:8]1)=[O:5])=[CH2:1].[C:4]([O:6][CH2:7][CH2:8][CH2:9][CH3:10])(=[O:5])[CH:2]=[CH2:1].[CH3:3][C:2]([C:4]([O:6][CH:7]1[C@@:12]2([CH3:16])[C:13]([CH3:15])([CH3:14])[C@H:9]([CH2:10][CH2:11]2)[CH2:8]1)=[O:5])=[CH2:1]

Participants

3

Reactant 1

HCID 71311141Isobornylmethacrylate

Product 1

HCID 131718422HCID 131718422, compound

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

Into a 355 ml clear flint glass bottle were charged 46 parts of polybutyl acrylate-XDC, [I(BT)n ], prepared according to the method of Example 7, 5 parts of isobornyl methacrylate, and 76.5 parts of ethyl acetate. The solution was purged and irradiated and the polymer isolated and dried as described in Example 7.

Workup

  1. customprepared
  2. customThe solution was purged
  3. customirradiated
  4. customthe polymer isolated
  5. customdried

Sources & evidence

ORD record
ord-742a6d0fab004302ae723e4c5c751211
Source dataset
uspto-grants-1994_06
Patent number
US05318999

Reaction notes

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