Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Caprolactam | HCID 7768 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86610174 | HCID 86610174 | — |
Reaction Steps
To a 100 ml flask containing 11.32 g of ε-caprolactam (0.1 mol), 30 ml water was added and stirred for dissolution. Then 21.95 g 40% aqueous solution of tetrafluoroboric acid (0.1 mol) was added dropwise into the flask over 20 min at room temperature. Then the reaction was stirred for another 1 hour. Desired product was formed after water was removed under reduced pressure and then dried at 110° C. under 1–5 mmHg for 1 hour. The yellowish, moisture- and water-stable liquid of N-protonated caprolactam tetrafluoroborate was obtained with a yield of 98.0%, which has a glass transition temperature of −78.2° C., a density of 1.34 g/ml, a viscosity of 503 cP, an electrochemical window of 2.0V, an ionic conductivity of 5.6×10−4 S/cm, and a Hammett acidic scale H0 of 2.56 using 2,4-dinitroaniline as indicator. No melting point was observed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07220869B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-3a29a2827b89422b979316044bdc1760 |
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| Source note | uspto-grants-2007_05 |
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