Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | Diglycidyl ether | HCID 16704 | — |
Reaction Steps
5.28 g of a phenol derivative represented by the following formula: ##STR19## 11.55 g of S-(+)-epichlorohydrin (chemical purity: 98.5% or more, optical purity: 99% or more), 3.00 g of potassium tert-butoxide and 45 ml of tert-butyl alcohol were mixed and stirred for 3 hours at 60° C. After evaporating the solvent from the reaction mixture at reduced pressure, the resultant was subjected to extraction with chloroform followed by evaporation of the solvent. The residue was purified by a silica gel column chromatography to obtain 5.82 g of a R-isomer of glycidyl ether represented by the following formula (Intermediate 2). ##STR20##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05507975 |
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| Source dataset | uspto-grants-1996_04 |
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| ORD ID | ord-bd2d605b7e4a42cbb2cce7ffa94eac09 |
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| Source note | uspto-grants-1996_04 |
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