HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Methyl 4-methoxy-2-(1-methylacetonyl)-acetoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-2-butanone | HCID 20026 | — |
| Reactant | Methyl 4-methoxyacetoacetate | HCID 123500 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 4-methoxy-2-(1-methylacetonyl)-acetoacetate | HCID 19871668 | 42% |
Reaction Steps
16.58 g (120 mmol) of potassium carbonate and 0.46 g (2 mmol) of benzyltriethylammonium chloride are suspended in 50 ml of acetonitrile. While stirring there are added thereto 14.60 g (100 mmol) of methyl 4-methoxyacetoacetate and there are added dropwise thereto within 10 minutes 15.97 g (150 mmol) of 3-chloro-2-butanone. The mixture is stirred at 20°-25° C. for a further 65 hours. The reaction mixture is poured on to 70 ml of 4N HCl/ice (pH value=1) and extracted 3 times with 100 ml of ethyl acetate each time. The combined organic phases are dried over magnesium sulphate and concentrated on a rotary evaporator. The crude product distils at 95° C./0.05 mbar and gives 6.67 g (42%) of methyl 4-methoxy-2-[1-methylacetonyl]-acetoacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892966 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-411e00c5ef8d4e01915a38867e01c4ac |
| Source note | uspto-grants-1990_01 |