HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → Diglycidyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Phenyl glycidyl ether | HCID 31217 | — |
| Product | Diglycidyl ether | HCID 16704 | — |
Reaction Steps
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##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04284574 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-6c48862f32dc478da666ce830cd63cb9 |
| Source note | uspto-grants-1981_08 |