HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Methyl 4-methoxy-2-(2-oxobutyl)-acetoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Chloromethyl ethyl ketone | HCID 69219 | — |
| Reactant | Methyl 4-methoxyacetoacetate | HCID 123500 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 4-methoxy-2-(2-oxobutyl)-acetoacetate | HCID 19871666 | 55.3% |
Reaction Steps
67.99 g (492 mmol) of potassium carbonate and 1.87 g (8.2 mmol) of benzyltriethylammonium chloride are suspended in 500 ml of acetonitrile. 59.86 g (410 mmol) of methyl 4-methoxyacetoacetate are added thereto while stirring. 65.50 g (615 mmol) of 1-chloro-2-butanone are added dropwise thereto within 30 minutes and the mixture is stirred at 20°-25° C. for 23 hours. The reaction mixture is poured into 1 l of 1N HCl (pH value=1) and extracted 3 times with 700 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 115° C./0.05 mbar. There results 49.01 g (55.3%) of methyl 4-methoxy-2-(2-oxobutyl)-acetoacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892966 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-c2d9b271073d4816982f12d4f1820928 |
| Source note | uspto-grants-1990_01 |