Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | HCID 39872367 | HCID 39872367 | — |
| Product | HCID 178487932 | HCID 178487932 | 117.5% |
Reaction Steps
A solution of trifluoro-3-oxa-butyrate (14.95 g, 81 mmol) and PPA (72 ml) was heated at 100° C. and then treated with p-anisidine (10 g, 81 mmol) portion wise. The reaction mixture was further heated to 150° C. and stirred for 2 h at 150° C. After cooling to RT, the reaction mixture was poured into a beaker containing ice water. After stirring for 20 min, the mixture was filtered, and the resulting solid was washed with water (˜3 L). The resulting pinkish-purple solid was dried under vacuum to provide 6-methoxy-2-(trifluoromethyl)quinolin -4-ol (11.58 g, 47.6 mmol, 58.6% yield), which was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987195B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-dd92160ac76f4788a2162434c054664f |
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| Source note | uspto-grants-2015_03 |
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