Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | HCID 59475970 | HCID 59475970 | — |
| Catalyst | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 59475971 | HCID 59475971 | 85.4% |
Reaction Steps
Trifluoromethanesulfonic acid (0.5 g, 0.0033 mol) was added slowly to a stirred solution of Example 4B (104 g, 0.211 mol) and triethylsilane (66.8 g, 0.574 mol) in trifluoroacetic acid (300 mL) cooled to 30° C. in a water-bath. The reaction became refluxed. After 0.5 h, the water bath was replaced by an oil bath. The reaction mixture was heated to reflux for 3 h. After cooling to room temperature, the reaction mixture was allowed to stir for another 1 h. The solid was filtered, washed with hexane (100 mL) and dried under vacuum at 30° C. to get the desired product as a pale gray solid (86.4 g, yield 85%) 1H NMR (CDCl3, 400 MHz): δ 7.2˜87.34 (m, 3H), 7.18˜7.25 (m, 4H), 4.08 (s, 1H), 2.93˜2.98 (m, 1H), 2.13-˜2.17 (m, 1H), 2.00˜2.03 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08283454B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-214e5a5913ff485790fab61b9a0b13e3 |
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| Source note | uspto-grants-2012_10 |
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