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HRID 1666115Erstellt: 26. Oktober 2026

Diethyl Ether → 5-(2,3-Difluorophenyl)nona-1,8-dien-5-ol

https://huagongshe.com/reaction/1666115

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
Edukt4-Iodobut-1-eneHCID 543216—
EduktBenzoic acid, 2,3-difluoro-, ethyl esterHCID 2761174—
EduktHCID 178418306HCID 178418306—
Produkt5-(2,3-Difluorophenyl)nona-1,8-dien-5-olHCID 57911455—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

In a 500 mL round-bottomed flask (t=g) was added crude 4-iodobut-1-ene (11.51 g, 63.2 mmol) in Et2O (100 mL) to give a colorless solution. After cooling to −78° C. under nitrogen, tBuLi (80 mL, 136 mmol) was added dropwise via syringe. The mixture was slowly warmed up to room temperature while stirring for 2 hours. After 20 minutes at room temperature, the mixture was cooled to −78° C. and ethyl 2,3-difluorobenzoate (4.28 mL, 28.7 mmol) was added dropwise via syringe. The mixture was gradually warmed up to room temperature over 30 minutes. The reaction was quenched by water and the volatiles were evaporated. The residue was partitioned between water and EtOAc. The layers were separated and the organic layer was washed with brine, dried with Na2SO4 and concentrated to a light yellow oil. Purification up to 40% Et2O in hexane afforded the desired product as a colorless oil: (1.41 g, 19%). 1H NMR (400 MHz, CDCl3) δ 7.31-7.22 (m, 1H), 7.10-7.03 (m, 2H), 5.82-5.70 (m, 2H), 4.97-4.85 (m, 4H), 2.20-2.00 (m, 4H), 2.00-1.75 (m, 4H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08044043B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-4ba70f0bd66e48d398cdfabbfd6f4952
Quellennotizuspto-grants-2011_10