Ethyl Methacrylate → HCID 19991765, compound

HRID 346000Notes

Reaction equation

HRID 346000 reaction equation
[O:1]1[CH2:6][CH2:5][N:4]([C:7]2[N:12]=[C:11]([N:13]3[CH2:18][CH2:17][O:16][CH2:15][CH2:14]3)[N:10]=[C:9]([N:19]3[C:24]([CH3:26])([CH3:25])[CH2:23][CH:22]([OH:27])[CH2:21][C:20]3([CH3:29])[CH3:28])[N:8]=2)[CH2:3][CH2:2]1.[C:30](OCC)(=[O:34])[C:31]([CH3:33])=[CH2:32].C(C1C(O)=C(C(C)(C)C)C=C(C)C=1)(C)(C)C>>[O:1]1[CH2:2][CH2:3][N:4]([C:7]2[N:12]=[C:11]([N:13]3[CH2:14][CH2:15][O:16][CH2:17][CH2:18]3)[N:10]=[C:9]([N:19]3[C:20]([CH3:29])([CH3:28])[CH2:21][CH:22]([O:27][C:30](=[O:34])[C:31]([CH3:33])=[CH2:32])[CH2:23][C:24]3([CH3:25])[CH3:26])[N:8]=2)[CH2:5][CH2:6]1

Participants

4

Procedure

10.2 g of 2,4-dimorpholino-6-(4-hydroxy-2,2,6,6-tetramethylpiperidin-1-yl)-1,3,5-triazine (product from Example 34) are heated to 120° together with 6.9 ml of ethyl methacrylate, 0.04 g of 2,6-bis-tert-butyl-p-cresol and 0.04 ml of tetrabutylorthotitanate (monomer), some liquid slowly being removed by distillation. The mixture is allowed to react for 50 hours, some ethyl methacrylate and catalyst subsequently being added periodically. After the reaction has ended, the product is filtered through bleaching earth and evaporated. The residue is dissolved in toluene/acetone and purified chromatographically on an SiO2 column, the above product being obtained as a colorless resin.

Workup

  1. customsome liquid slowly being removed by distillation
  2. customto react for 50 hours
  3. filtrationthe product is filtered
  4. customevaporated
  5. dissolutionThe residue is dissolved in toluene/acetone
  6. custompurified chromatographically on an SiO2 column
  7. customthe above product being obtained as a colorless resin

Sources & evidence

ORD record
ord-435a24ede1b94759b75c06e71ad030c4
Source dataset
uspto-grants-1991_10
Patent number
US05059689

Reaction notes

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