HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → t-Butyl 2-(6-cyano-2-naphthyloxy)-5-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Hydroxy-2-naphthonitrile | HCID 4589476 | — |
| Reactant | Tert-butyl 2-fluoro-5-nitrobenzoate | HCID 22380964 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | t-Butyl 2-(6-cyano-2-naphthyloxy)-5-nitrobenzoate | HCID 22380917 | — |
Reaction Steps
The compound (t-butyl 2-fluoro-5-nitrobenzoate) (1.74 g) obtained in a previous production example, 6-cyano-2-naphthol (1.86 g) and potassium carbonate (8.2 g) were heated to 50° C. in N,N-dimethylformamide and reacted for 2 hours. After cooling to room temperature, water was added and extraction was performed with ethyl acetate. The ethyl acetate layer was washed with saturated saline and dried over magnesium sulfate, and the solvent was distilled off. The residue was purified by silica gel chromatography (300 g, hexane:ethyl acetate=5:1) to obtain 3.23 g of t-butyl 2-(6-cyano-2-naphthyloxy)-5-nitrobenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06916837B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-963d3e736c7340afb56855abd981d7af |
| Source note | uspto-grants-2005_07 |