HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 19093454, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | HCID 136378379 | HCID 136378379 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19093454 | HCID 19093454 | — |
Reaction Steps
2 Equivalents of triethylamine are added to a suspension of the oxime in dry methylene chloride at -78° under nitrogen. 1.1 equivalent of triflic anhydride are then added dropwise over 3 minutes. After stirring overnight, the reaction mixture is diluted with ethyl acetate and washed with 10% sodium bicarbonate solution. The organic phase is dried over anhydrous magnesium sulfate. Solvent removal provides the desired 3-cyano-7-bromo-4-aza-9-fluorenone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05294610 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-6da7be05766a44a2a3c55f9ed82f3e8a |
| Source note | uspto-grants-1994_03 |