HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893539Generated: October 28, 2026
Ethyl 3-(trifluoromethyl)non-2-enoate → HCID 54107361, compound
https://huagongshe.com/reaction/893539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 3-(trifluoromethyl)non-2-enoate | HCID 53647231 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54107361 | HCID 54107361 | 112.5% |
Reaction Steps
13.78 g of ethyl 3-trifluoromethyl-2-nonenoate was dissolved in 138 ml of methanol, and 1.38 g of 5%-palladium/activated carbon was added thereto, followed by stirring for 4 hours at room temperature and normal pressure in a hydrogen atmosphere in a catalytic hydrogenation apparatus. After the reaction, the 5%-palladium/activated carbon was filtered out, and the remaining methanol solution was mixed with 24 ml, of water and 20 g of potassium hydroxide, followed by 2 hours of heat refluxing, distilling-off of methanol under a reduced pressure, acidification with addition of 6N-hydrochloric acid, and extraction with methylene chloride. The resultant methylene chloride solution was dried on sodium sulfate, followed by distilling-off of the solvent and purification by distillation (b.p.: 118.5°-119.7° C./20 mmHg), whereby 13.78 g of 3-trifluoromethylnonenoic acid was obtained. (Yield: 51.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05126071 |
|---|
| Source dataset | uspto-grants-1992_06 |
|---|
| ORD ID | ord-7e42de5ea2f7456ea685722f668877aa |
|---|
| Source note | uspto-grants-1992_06 |
|---|