HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Phenylprop-2-Enal → Cinnamaldehyde, thiosemicarbazone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Phenylprop-2-Enal | HCID 307 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Solvent | Water | HCID 962 | — |
| Product | Cinnamaldehyde, thiosemicarbazone | HCID 2737765 | — |
Reaction Steps
A solution of 18.2 g (0.20 m) of thiosemicarbazide in 250 ml of hot water was gradually added to a solution of 26.4 g (0.20 m) of cinnamaldehyde in 250 ml of hot 2B ethanol. Small, colorless crystals began to ppt from the homogeneous mixture after several minutes of heating on a steam bath. Heating was continued for a half an hour, after which the mixture was cooled to room temperature and the product was collected by filtration, washed with cold ethanol, and air-dried to yield 25.5 g of small, pale yellow crystals. An additional 18.3 g of product was recovered by concentrating the mother liquors. Recrystallization from ethanol gave 29.3 g (0.14 m) of small, pale yellow crystals, m.p. 137°-139° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04219475 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-bbde15da2f904e8abc541e1519ad99bb |
| Source note | uspto-grants-1980_08 |