Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 54320035 | HCID 54320035 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22034106 | HCID 22034106 | 105.2% |
Reaction Steps
A mixture of trifluoro-methanesulfonic acid 2-methyl-8-(2,4,6-trimethyl-phenyl)-quinolin-4-yl ester (426 mg, 1 mmol) and potassium bromide (KBr) (809 mg, 1.1 mmol) in a mixture of 1 ml of dry DMSO and 3 ml of dry THF was heated in 120° C. oil bath for 3 hours. The mixture was quenched with water, extracted with ethyl acetate. The organic layer was dried and concentrated to give 358 mg of the title compound as an off-white solid. 1H NMR (CDCl3) δ 8.16 (m,1H), 7.59 (m,1H), 7.56(s,1H), 7.48(m,1H), 6.97(s,1H), 2.53(s,3H), 2.37(s,3H), 1.87(,6H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06875769B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-700c5712e9134bbd859af4436c10d433 |
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| Source note | uspto-grants-2005_04 |
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