HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738736Generated: November 1, 2026
Triethylamine → 2-Fluoro-2-trifluoromethyl-4-octenamide
https://huagongshe.com/reaction/1738736
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (3R)-1-hexen-3-ol | HCID 6992421 | — |
| Reactant | Ethanamine, N-ethyl-, compd. with 1,1,2,3,3,3-hexafluoro-1-propene (1:1) | HCID 11770067 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Fluoro-2-trifluoromethyl-4-octenamide | HCID 53835303 | — |
Reaction Steps
Into a reaction flask were charged 920 mg of (R)-1-hexen-3-ol (91.2%e.e.), 5.7 ml of triethylamine and 10 ml of dichloromethane, and the reaction mixture was cooled to 0° C. Holding the temperature at 0° C., 3.3 ml of hexafluoropropene diethylamine was added dropwise into the mixture. After the addition, the reaction mixture was stirred for 2 hours at 0° C. and 48 hours at room temperature. Into the mixture was added a saturated aqueous solution of sodium bicarbonate, and the mixture was extracted with dichloromethane. The organic layer was dried with anhydrous magnesium sulphate and then concentrated. The raw product was purified by silica gel column chromatography to obtain 1.35 g of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05965059 |
|---|
| Source dataset | uspto-grants-1999_10 |
|---|
| ORD ID | ord-1da0ef9cacfe4137a2d2e53cb63badc6 |
|---|
| Source note | uspto-grants-1999_10 |
|---|