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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086095Generated: November 1, 2026

Tetrahydrofuran → 4-Ethyl-5,5-bis(4-fluorophenyl)-2,4-pentadienal

https://huagongshe.com/reaction/1086095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantCyclohexylisopropylamineHCID 62386—
Reactant2-Ethyl-3,3-bis(4-fluorophenyl)-2-propenalHCID 15133055—
ReactantButyllithiumHCID 178418339—
Product4-Ethyl-5,5-bis(4-fluorophenyl)-2,4-pentadienalHCID 54118635—

Reaction Conditions

Temperature-40 °C

Reaction Steps

Butyl lithium (25.7 mL of 2.1M solution, 54 mmol) was added to a solution of N-isopropylcyclohexylamine in 30 mL tetrahydrofuran at -10° C. After stirring for 30 minutes and cooling to -40° C., N-ethylidenecyclohexamine (27 mL of 2M solution, 54 mmol) was added and the solution stirred for 30 minutes. The solution was further cooled to -70° C. and 2-ethyl-3,3-bis(4-fluorophenyl)- 2-propenal(4.9 g, 18 mmol) in 40 mL of tetrahydrofuran was added. The mixture was stirred for 5 hours and quenched with water. The mixture was extracted with diethyl ether, the extracts dried over magnesium sulfate and concentrated in vacuo. The residue was stirred with a mixture of 100 mL of benzene, 40 mL of water and 60 mL of acetic acid for 16 hours and diluted with 1.50 mL of water. The organic layer was separated, washed with saturated sodium bicarbonate solution, dried with magnesium sulfate and concentrated in vacuo. The residue was crystallized from petroleum ether to give 3.45 g of the title compound; m.p. =98°-99.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011947
Source datasetuspto-grants-1991_04
ORD IDord-a7484ae1758648afa9b616e848bfae06
Source noteuspto-grants-1991_04