Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Methylquinoline | HCID 7059 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Product | 6-Quinolinecarbaldehyde | HCID 765653 | 20% |
Reaction Steps
A mixture of SeO2 (10.89 g, 99 mmol) and 6-methylquinoline (12.87 g, 90 mmol) was heated to 150° C. and stirred for 16 h. Then it was cooled to room temperature and EtOAc (400 ml) was added. After filtration, the filtrate was concentrated to obtain the crude compound, which was purified by chromatography (silica gel, petroleum ether/EtOAc 5:1 to 2:1) to afford the title compound (2.87 g, yield 20%). LC-MS (ESI) m/z: 158 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420650B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-9f12b031fd7849c289b35caa45d03420 |
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| Source note | uspto-grants-2013_04 |
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