Reaction equation
[C:1]1([CH:8]=[CH:7][CH:6]=[C:4]([OH:5])[CH:3]=1)O.[C:9]1([CH:16]=[CH:15][C:13]([OH:14])=[CH:12][CH:11]=1)O.C[C:18]1[C:24](O)=[CH:23][CH:22]=[CH:21][C:19]=1[OH:20].OC1C=C[C:30]([C:31]([C:33]2[CH:38]=[CH:37][C:36]([OH:39])=[CH:35][CH:34]=2)=O)=CC=1.OC1C2C(=[C:48]([OH:53])[CH:49]=[CH:50]C=2)C=CC=1.OC1C=CC(C(C2[CH:69]=[CH:68][C:67]([OH:70])=CC=2)(C)C)=CC=1.[OH:71][C:72]1[CH:77]=CC(C(C2C=CC(O)=CC=2)CC)=C[CH:73]=1.[OH:88][C:89]1[CH:94]=CC(C(C2C=CC(O)=CC=2)C)=C[CH:90]=1.O[C:105]1C=CC(C(C2C=CC(O)=CC=2)C(C)C)=CC=1.OC1C=CC(C(C2C=CC(O)=CC=2)(CC)C)=CC=1.OC1C=CC(C(C2C=CC(O)=CC=2C)(C)C)=C(C)C=1.OC1C=CC(C(C2C=CC(O)=CC=2)(CC)CC)=CC=1.OC1C=CC(C(C2C=CC(O)=CC=2)C(CC)CCCC)=CC=1.OC1C=CC(CC2C=CC(O)=CC=2)=CC=1>>[O:5]([CH2:90][CH:89]([O:88][CH2:50][CH:49]1[O:53][CH2:48]1)[CH2:94][O:14][C:13]1[CH:15]=[CH:16][C:9]([C:31]([C:33]2[CH:34]=[CH:35][C:36]([O:39][CH2:73][CH:72]([O:71][CH2:69][CH:68]3[O:70][CH2:67]3)[CH2:77][O:20][C:19]3[CH:18]=[CH:24][CH:23]=[CH:22][CH:21]=3)=[CH:37][CH:38]=2)([CH3:30])[CH3:105])=[CH:11][CH:12]=1)[C:4]1[CH:6]=[CH:7][CH:8]=[CH:1][CH:3]=1Participants
Reactant 14
Product 1
Procedure
Suitable polyethers of polyhydric phenols excluding the diglycidyl ethers noted above, include for example, the polyglycidyl polyethers of dihydric phenols including mononuclear phenols such as resorcinol, catachol, hydroquinone and methyl resorcinol and polynuclear phenols such as 4,4'-dihydroxy benzophenone, 1,5-dihydroxy naphthalene and particularly the alkylene bis-phenols such as 2,2-bis(4-hydroxyphenyl)propane, 1,1-bis(4-hydroxyphenyl)propane, 1,1-bis(4-hydroxyphenyl)ethane, 1,1-bis(4-hydroxyphenyl)isobutane, 2,2-bis(4-hydroxyphenyl)butane, 2,2-bis(4-hydroxy-2-methylphenyl)propane, 1,1-bis(4-hydroxyphenyl)-2-methyl propane, 3,3-bis(4-hydroxyphenyl)pentane, 1,1-bis(4-hydroxyphenyl)2-ethylhexane, and bis(4-hydroxyphenyl)methane.
Sources & evidence
- ORD record
- ord-0414fbd0bc7b42eaa0af1d4210d1c00e
- Source dataset
- uspto-grants-1989_07
- Patent number
- US04845172
Linked notes
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