Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 4-Chlorotoluene | HCID 7810 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | Phenylacetic Acid | HCID 999 | 94.1% |
Reaction Steps
In accordance with the process of Example 1, 12.7 g of p-chlorotoluene were contacted and reacted with 5.4 g of sodium dispersed in 50 ml of cyclohexane at 20° C to 30° C and then the reaction mixture was heated to 80° C for 5 hours to rearrange the product. The reaction mixture was cooled to 20° C to 23° C and was gradually poured onto 10 g of solid carbon dioxide with stirring to effect the carbonylation reaction. After the reaction with carbon dioxide, the post-treatment procedure was conducted in accordance with the process of Example 1 to whereby 12.8 g of phenylacetic acid (yield 94.1%) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04084061 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-dd13c31fe78346f49905649bf3ad16f1 |
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| Source note | uspto-grants-1978_04 |
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