Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Tert-butyl acetoacetate | HCID 15538 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 13157028 | HCID 13157028 | 96% |
Reaction Steps
5 ml of tetrachloromethane were added to 24.3 g (1 mol) of magnesium turnings in 50 ml of dry ethanol under nitrogen and in the absence of moisture. After the beginning of gas evolution, a solution of 177.7 g (1 mol) of tert-butyl acetoacetate in 100 ml of dry ethanol was slowly added dropwise, the reaction mixture being kept at reflux temperature. Stirring was carried out for a further 4 hours at this temperature, after which the mixture was cooled. 78.5 g (1 mol) of benzoyl chloride was slowly added dropwise at 10° C. Stirring was continued for a further 4 hours at room temperature and hydrolysis was then effected with a mixture of 450 ml of ice water and 25 ml of concentrated sulfuric acid. The organic phase was separated off, dried, and evaporated down under reduced pressure. 192.3 g of >96% pure tert-butyl 2-benzoylacetoacetate were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05338639 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-2ad2235c18c24c37aa93a5b3b49eec8f |
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| Source note | uspto-grants-1994_08 |
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