Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 1-Propanol, 2-(2-(2-methoxypropoxy)propoxy)- | HCID 25054 | — |
| Reactant | HCID 86592450 | HCID 86592450 | — |
| Product | Boric Acid | HCID 7628 | — |
| Product | Trimethyl borate | HCID 8470 | — |
Reaction Steps
207.6 Grams (2.0 mols) of trimethyl borate was added to 202 g (1.0 mol) of dipropylene glycol monomethacrylate and 412 g (2.0 mols) of tripropylene glycol monomethyl ether, followed by keeping them at 60° C. for 1 hour with stirring in a dry air atmosphere and then heating to 75° C. After the temperature reached 75° C., the pressure in the system was gradually reduced. The system was kept at a pressure of 2.67 kPa (20 mmHg) or lower for 6 hours to remove volatile matters produced with progress of ester interchange reaction of boric acid and excess trimethyl borate, followed by filtration to obtain 610 g of the polymerizable boron-containing compound B represented by the formula (1). An infrared absorption spectrum of the resulting polymerizable boron-containing compound B was measured to confirm that the absorption band originating from hydroxyl group at 3300 cm−1 disappeared.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07473492B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-45a32ace41d843a389edef54d2ec11c9 |
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| Source note | uspto-grants-2009_01 |
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