Methyl Methacrylate → HCID 100936470, compound

HRID 1462572Notes

Reaction equation

HRID 1462572 reaction equation
[CH3:1]OC(=O)C(C)=C.O=[C:9]1O[C@H:14]([C@H:16]([CH2:18]O)[OH:17])[C:12](O)=[C:10]1O.C1[C:26](=[N:27][C:28]2[CH:33]=[CH:32][C:31]([NH2:34])=[CH:30][CH:29]=2)C=CC(=O)C=1>C1(C)C=CC=CC=1.C(O)CCC.C(O)C>[CH3:1][N:27]([C:28]1[CH:29]=[CH:30][C:31]([NH:34][CH:10]2[CH:9]=[CH:18][C:16](=[O:17])[CH:14]=[CH:12]2)=[CH:32][CH:33]=1)[CH3:26]

Participants

7

Reactant 3

HCID 6658Methyl MethacrylateHCID 24748760IndoanilineHCID 54670067L-Ascorbic Acid2×

Product 1

HCID 100936470HCID 100936470, compound

Reagents, catalysts & solvents 3

HCID 2631-ButanolSolventHCID 702EthanolSolventHCID 1140TolueneSolvent

Procedure

The fifth layer consisted of the magenta/cyan barrier polymer and the magenta reactants. A polymer premix was prepared by dissolving 64.5 g of a methylmethacrylate polymer in 178.5 g of toluene and 15.05 g of n-butyl alcohol. The leuco indoaniline magenta developer was prepared by reducing the dye with ascorbic acid. This was done by dissolving 0.63 g of ascorbic acid in 45 g of ethanol. Then 1.2 g of the magenta indoaniline dye was added. ##STR22##

Workup

  1. additionA polymer premix
  2. customwas prepared

Sources & evidence

ORD record
ord-138932d2fa2a4d56b3de989f20205d28
Source dataset
uspto-grants-1984_07
Patent number
US04460681

Reaction notes

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