HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539388Generated: October 25, 2026
Chloride → 5-Norbornene 2-methylcinnamate
https://huagongshe.com/reaction/539388
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Bicyclo(2.2.1)hept-5-ene-2-methanol | HCID 78946 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Norbornene 2-methylcinnamate | HCID 86606457 | 88% |
Reaction Steps
15 g (0.121 mol) of the 5-norbornene-2-methanol prepared in Example 1, 61.2 g (0.605 mol) of triethylamine (produced from Aldrich Inc.), and 20 ml of THF were loaded into a 250 ml 2-neck flask and then stirred at 0° C. in an ice-water bath. 22.1 g (0.133 mol) of cinamoil chloride dissolved in 60 ml of THF was slowly added to the prepared mixture using an additional flask for 10 minutes. Then, the temperature of the reactant was increased to room temperature and then stirred for one hour. The resulting solution was diluted using an ethyl acetate. The diluted solution was loaded into a separatory funnel, washed using water and NaHCO3 several times, and then distilled in at a reduced pressure to remove a solvent. The result was refined using a column chromatography (Hexane: Ethyl acetate=20:1) to attain a product. (Yield: 88%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | USRE045219E1 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-b12ebf1f8c3b405fb78ffbe9a5a21978 |
|---|
| Source note | uspto-grants-2014_10 |
|---|