HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Coumaric acid → P-hydroxyl ethyl cinnaMate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Coumaric acid | HCID 322 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Product | P-hydroxyl ethyl cinnaMate | HCID 349172 | — |
Reaction Steps
To a solution of 4- hydroxycinnamic acid (16.4 g) in ethanol (100 ml) was added sulfuric acid (10 ml). The mixture was refluxed with heating for 4 hours, Aqueous sodium bicarbonate solution was added to the reaction solution so as to make basic. Then, the reaction solution was extracted with chloroform. The extract was dried over sodium sulfate anhydride and then concentrated under a vacuum to yield a raw product of ethyl 4-hydroxycinnamate. In a manner similar to Reference Example 1, this raw product was reacted with geranyl bromide (21.7 g) and then hydrolyzed to yield 13.9 g (46%) of 4-geranyloxycinnamic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05849930 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-2d31f033a34d4c49b4c78350e5e55120 |
| Source note | uspto-grants-1998_12 |