HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 53629726, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 58345633 | HCID 58345633 | — |
| Product | HCID 53629726 | HCID 53629726 | — |
Reaction Steps
To a mixture of 2-(2-fluorobenzoyl)-4,5-dihydroxy-3-nitrobenzonitrile (compound 1-29) (70 mg) and tetrahydrofuran (2.0 mL) were added ethyl chlorocarbonate (70 μl) and triethylamine (110 μl) under ice-bath cooling. After stirring for 30 minutes, the mixture was stirred at room temperature for 2 days. The mixture was diluted with ethyl acetate, and washed with 1 mol/L hydrochloric acid and brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: 0%-30% ethyl acetate/hexane, gradient elution) to give the title compound (103 mg). The structural formula was illustrated in table 10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08258162B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-0424a95e9321478f9367e971821461db |
| Source note | uspto-grants-2012_09 |