Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Mesitylene | HCID 7947 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | 1,2,3-Trifluoro-4-nitrobenzene | HCID 69871 | — |
| Reactant | Sodium 2-methylbutan-2-olate | HCID 2733478 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 67440835 | HCID 67440835 | — |
Reaction Steps
Sodium tert-pentoxide (33.52 g) was added to mesitylene (280 ml) and the mixture heated to 50° C. To the suspension was added ethyl acetoacetate (39.61 g) over 10 minutes. The reaction mixture exothermed to about 60° C. The thick slurry was heated to 70° C. and 1,2,3-trifluoro-4-nitrobenzene (25.0 g) added. The mixture exothermed to 80° C. The mixture was held at 70-80° C. for 3 hours, then allowed to cool to ambient and left overnight. To the mixture was added hydrochloric acid (6% w/w, 100 ml), until the pH reached 1. The aqueous layer was separated and discarded and the organic layer washed twice with hydrochloric acid 6% w/w, 90 ml), then with aqueous sodium bicarbonate (2.3% w/w, 37.5 ml) and finally water (75 ml). To the organic layer was added further mesitylene (53 ml) and the mixture distilled on a rotary evaporator (10 mbar, bath 60° C.) to give a solution of ethyl 2-(2,3-difluoro-6-nitrophenyl)-3-oxobutanoate in mesitylene (90 ml containing 36.22 g of ethyl 2-(2,3-difluoro-6-nitrophenyl)-3-oxobutanoate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08754240B2 |
|---|
| Source dataset | uspto-grants-2014_06 |
|---|
| ORD ID | ord-8abcd24d6fe74bbd9a267190beb5635d |
|---|
| Source note | uspto-grants-2014_06 |
|---|