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 | — |
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 gylcidyl 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 |
|---|
| Patent number | US08071706B2 |
|---|
| Source dataset | uspto-grants-2011_12 |
|---|
| ORD ID | ord-be5f9d3b8e6147cea19c563023c3b2f5 |
|---|
| Source note | uspto-grants-2011_12 |
|---|