Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl glycidyl ether | HCID 7838 | — |
| Reactant | Hydride | HCID 166653 | — |
| Reactant | Alumina | HCID 9989226 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Diglycidyl ether | HCID 16704 | 87.2% |
Reaction Steps
Allyl glycidyl ether (13.2 mL, 0.111 mol) was added to HMS-501 (10.0 g, 0.0741 mol) in toluene. A catalytic amount of PtO2 was added, and the mixture was heated at 90° C., overnight. An NMR spectrum taken the following day showed there to be substantially no remaining hydride (peak at approx. 4.7 ppm). The reaction mixture was then cooled and passed through a bed of aluminum oxide layered on top of a fitted glass filter. The frit was washed with additional toluene. The eluent was collected in a round-bottom flask. The solvent and residual allyl glycidyl ether were then removed in vacuo at 50° C., to yield the epoxy-PDMS as a thick clear liquid (16.09 g, 87.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08283432B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-e0f8057211b64b178e04a1898a5229ce |
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| Source note | uspto-grants-2012_10 |
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