Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 4-Hydroxy-3-nitro-5,6,7,8-tetrahydroquinolin-2(1H)-one | HCID 54684515 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54000465 | HCID 54000465 | 93.2% |
Reaction Steps
Trifluoromethanesulfonic anhydride (8.0 mL, 47 mmole) was added via a syringe to a cooled (0° C.) homogeneous mixture containing 5,6,7,8-tetrahydro-4-hydroxy-3-nitro-2(1H)-quinolinone (4.0 g, 19 mmole) and triethylamine (6.6 mL, 47 mmole) in methylene chloride (200 mL). The reaction mixture was stirred at 0° C. for 30 minutes. The reaction mixture was filtered through a layer of silica gel and the gel eluted with methylene chloride. The organic phase was evaporated under vacuum to provide 8.4 g of the desired product as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05444065 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-18874fdff4d849c8b72797313660a179 |
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| Source note | uspto-grants-1995_08 |
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