HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic anhydride → 4-((4-Methoxybenzyl)oxy)-6-(trifluoromethyl)quinoline-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 4-((4-Methoxybenzyl)oxy)-6-(trifluoromethyl)quinoline-2-carboxamide | HCID 58562851 | — |
| Product | 4-((4-Methoxybenzyl)oxy)-6-(trifluoromethyl)quinoline-2-carbonitrile | HCID 58562526 | — |
Reaction Steps
A solution of 4-((4-methoxybenzyl)oxy)-6-(trifluoromethyl)quinoline-2-carboxamide (9 g, 24 mmol) from above step B, and TEA (10 mL, 72 mmol) was treated with trifluoroacetic anhydride (4.35 mL, 31.3 mmol) at room temperature and stirred for 2 h (completion of reaction monitored by LCMS). Solvent was removed under vacuum and the residue was purified by recrystallization from EtOAc/Hex to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08518969B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-679d0b26dff14cc5a1f3a17c9c365ef2 |
| Source note | uspto-grants-2013_08 |