Phenol → Diglycidyl ether
Reaction equation
C1([OH:7])C=CC=CC=1.[CH2:8]([O:12][C:13]1[CH:18]=[CH:17]C=CC=1)[CH:9]1[O:11][CH2:10]1>>[CH2:13]([O:12][CH2:8][CH:9]1[O:11][CH2:10]1)[CH:18]1[O:7][CH2:17]1Participants
3
Reactant 2
Product 1
Procedure
Such a mono(chlorohydrin ether) as that of formula V is then mixed with up to an equimolar amount of a bis(chlorohydrin ether) of a polyhydric phenol, and subjected to dehydrochlorination. The materials obtained, described as synthetic high molecular weight products of resinous character, are of a complex nature and generally solids of melting point 43° C. or more. Presumably, if, e.g., phenyl glycidyl ether were used, the product obtained on dehydrochlorination would contain, amongst other compounds, a glycidyl ether of a mono-secondary alcohol formed in the following manner ##STR3##
Workup
- customThe materials obtained
- customthe product obtained on dehydrochlorination
Sources & evidence
- ORD record
- ord-6c48862f32dc478da666ce830cd63cb9
- Source dataset
- uspto-grants-1981_08
- Patent number
- US04284574
Reaction notes
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