HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Propenoic acid, 3-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Benzene, (1,3,3,3-tetrachloropropyl)- | HCID 90965 | — |
| Product | 2-Propenoic acid, 3-phenyl- | HCID 8784 | 9.8% |
Reaction Steps
A mixture of 51.6 g of 1,1,1,3-tetrachloro-3-phenylpropane, 60 g of glacial acetic acid and 17.8 g of 55% sulphuric acid is refluxed under stirring at 115° to 122° C. for 5 h, after which time the evolution of hydrogen chloride ceases. The work-up of the reaction mixture as described in Example 1 yields 22.5 g and 2.9 g of cinnamic acid in 85.8% total yield (melting point 131.5° to 133° C., min. 99% purity).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04806681 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-13167917bb734d70b8a04fb020b90512 |
| Source note | uspto-grants-1989_02 |