Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Propenoic acid, 3-phenyl-, methyl ester | HCID 7644 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-Propenoic acid, 3-phenyl- | HCID 8784 | 95.3% |
Reaction Steps
100 g of crude methyl cinnamate and 926.8 g of 2.8% caustic soda were placed in a 2-liter flask equipped with a thermometer and a stirrer, and the solution was then stirred at 80° C. for 30 minutes to carry out hydrolysis. An active carbon treatment was omitted. The abovementioned aqueous solution was maintained at 40° C., and 137.1 g of 25% sulfuric acid was added dropwise to precipitate the crystals of cinnamic acid. After the addition of sulfuric acid had been over, the temperature of the solution was lowered to 20° C., followed by filtering through Nutsche. The resultant filter cake was washed with 1000 g of water, and then vacuum-dried at 50° C. to obtain 87.1 g of cinnamic acid. The purity of cinnamic acid was 96.1%, and the contents of palladium, copper and manganese were 5 ppm or less, 260 ppm, 200 ppm, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05206430 |
|---|
| Source dataset | uspto-grants-1993_04 |
|---|
| ORD ID | ord-8dcced3d9d9d45508d857b348cf060f6 |
|---|
| Source note | uspto-grants-1993_04 |
|---|