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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Cyclohexylisopropylamine | HCID 62386 | — |
| Reactant | 2-Ethyl-3,3-bis(4-fluorophenyl)-2-propenal | HCID 15133055 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 4-Ethyl-5,5-bis(4-fluorophenyl)-2,4-pentadienal | HCID 54118635 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05011947 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-a7484ae1758648afa9b616e848bfae06 |
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| Source note | uspto-grants-1991_04 |
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