Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | HCID 86743802 | HCID 86743802 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86743801 | HCID 86743801 | 142.6% |
Reaction Steps
BMPDMS (260 mg), TASHF2 (100 microliters, 0.1 M. in CH3CH) and THF (125 mL) were added to a dry 250 mL 3-necked round-bottomed flask equipped with a magnetic stirrer, a thermocouple, a reflux condenser and a nitrogen bubbler and the mixture was cooled to 0° C. A solution of (±)-2,2'-((1,1'-binaphthalene)-2,2'-diylbis(oxy))-bis(ethanol) dimethacrylate (2.5 g, 4.9 mmole) and TASHF2 (100 μL, 0.1 M. in CH3CN) in THF (125 mL) were added dropwise (0.5 mL/min) to the solution in the 250 mL flask to give a yellow mixture. This mixture was stirred overnight at 0° C. and then condensed. Hexane was added, and the polymer which precipitated was dried to give 1.91 g of a white powdery solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04906713 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-8607c71f2759460e9a4add84050f23d7 |
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| Source note | uspto-grants-1990_03 |
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