HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Phenylacetic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Acetylacetonate | HCID 5460482 | — |
| Catalyst | Nickel | HCID 935 | — |
| Catalyst | Vanadium | HCID 23990 | — |
| Catalyst | Sodium orthovanadate | HCID 61671 | — |
| Catalyst | Nickel acetate tetrahydrate | HCID 62601 | — |
| Product | Phenylacetic Acid | HCID 999 | — |
Reaction Steps
Using the equipment and the procedure described for Example 1, an experiment was carried out on a charge comprising 25 ml (232 mmols) of benzyl alcohol, 15 ml of acetic acid, 161 mmols of methyl iodide, 8 mg atoms of nickel in the form of nickel acetate tetrahydrate and 40 mg atoms of vanadium in the form of vanadyl bis-acetylacetonate. The reaction temperature was 180° C.; the total pressure was maintained at 60 bars by introduction of additional amounts of pure CO. In a reaction time of 1 hour, 30 minutes at the temperature indicated, 15.8 g of phenylacetic acid were obtained (RY=48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04436889 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-4d2f53c018084bcf864a994af894fa93 |
| Source note | uspto-grants-1984_03 |