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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant(3R)-1-hexen-3-olHCID 6992421—
ReactantEthanamine, N-ethyl-, compd. with 1,1,2,3,3,3-hexafluoro-1-propene (1:1)HCID 11770067—
SolventDichloromethaneHCID 6344—
Product2-Fluoro-2-trifluoromethyl-4-octenamideHCID 53835303—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965059
Source datasetuspto-grants-1999_10
ORD IDord-1da0ef9cacfe4137a2d2e53cb63badc6
Source noteuspto-grants-1999_10