Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | HCID 68144010 | HCID 68144010 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Benzoylacetic acid | HCID 97045 | — |
Reaction Steps
6.7 g of potassium 2,6-di-t-butyl-p-cresolate in 30 cc of toluene were introduced into a 4-neck flask, having a capacity of 100 cc, provided with stirrer, thermometer and gas inlet pipe. In a carbon dioxide atmosphere 3.1 g of acetophenone (phenate: substrate molar ratio = 1 : 1) were added; the whole was stirred at 20°C for 4 hours and then acidified with cold sulphuric acid at 10% concentration. The organic phase separated, and was then extracted with a 10% sodium carbonate aqueous solution. 0.9 g of benzoylacetic acid were isolated by acidification and extraction with ether. 2.3 g of acetophenone were recovered from the organic phase.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03976677 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-5c32a81745d04192952fc09df2ada626 |
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| Source note | uspto-grants-1976_08 |
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