HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2-(chlorocarbonyl)-6-nitrobenzoate → Methyl 2-acetyl-6-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2-(chlorocarbonyl)-6-nitrobenzoate | HCID 12651086 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-acetyl-6-nitrobenzoate | HCID 59644399 | — |
Reaction Conditions
| Temperature | -20 °C |
|---|
Reaction Steps
To a suspension of copper(I)cyanide (5.70 g, 63.6 mmol) in 200 mL of anhydrous THF at −78° C. was added methyl magnesium bromide (1.4 M in toluene and THF, 43 mL, 59.3 mmol). The mixture was stirred at −20° C. for 20 min, then cooled to −78° C. A solution of 2-chlorocarbonyl-6-nitro-benzoic acid methyl ester (11.6 g, 47.8 mmol, Step B) in 30 mL of THF was added. The mixture was cooled at −10° C., and slowly warmed to RT, quenched with NH4Cl(aq), and extracted with EtOAc. The combined organic portions were washed with brine, dried over MgSO4, filtered, condensed, and purified by flash column chromatography, to provide the titled compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07320992B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-673a74252478423db9562632fdee041b |
| Source note | uspto-grants-2008_01 |