Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Cinnamic Acid | HCID 444539 | — |
| Catalyst | Tetraethylammonium Bromide | HCID 6285 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53975804 | HCID 53975804 | — |
Reaction Steps
To 7.5 g of trans-cinnamic acid (manufactured by Wako Pure Chemical) were added 3 g of tetraethylammonium bromide (manufactured by Wako Pure Chemical) and 100 ml of epichlorohydrin (manufactured by Wako Pure Chemical), the mixture was heated to reflux at 110° C. for 3 hours, 50 ml of distilled water was added thereto, an organic layer was separated, concentrated in vacuo at 80° C. and distilled under reduced pressure of 6 mmHg and the fraction of 130 to 160° C. was recovered to give 12 g of glycidyl cinnamate. An epoxy equivalent of this glycidyl cinnamate was 240.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08222399B2 |
|---|
| Source dataset | uspto-grants-2012_07 |
|---|
| ORD ID | ord-eebb9185c2de447c8ef1476e481019a7 |
|---|
| Source note | uspto-grants-2012_07 |
|---|