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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 920896Erstellt: 23. Oktober 2026

Phosphonium, (bromomethyl)triphenyl-, bromide (1:1) → (Z)-2-(2-bromovinyl)-6-fluoroquinoline

https://huagongshe.com/de/reaction/920896

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphonium, (bromomethyl)triphenyl-, bromide (1:1)HCID 2733422—
Edukt6-Fluoroquinoline-2-carbaldehydeHCID 3159605—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(Z)-2-(2-bromovinyl)-6-fluoroquinolineHCID 8668311365,4%

Reaktionsschritte

To as suspension of (bromomethyl)triphenylphosphonium bromide (14.94 g, 34.3 mmol) in 100 mL of THF was added potassium tert-butoxide (3.84 g, 34.3 mmol) portionwise under Ar. Then the reaction mixture was stirred for 1 h at this temperature. 6-Fluoroquinoline-2-carbaldehyde (5 g, 28.5 mmol) in 40 mL of THF was added. The resulting reaction mixture was stirred for 5 h at −75° C. and allowed to warm up overnight. The reaction mixture was diluted with petrol ether and the solid was sucked off. The mother liquid was concentrated, diisopropyl ether was added and the formed precipitate was sucked off. The mother liquid was purified by column chromatography (cyclohexane/EA) to give 4.7 g (65.3%) of the title compound as brown solid. LC-MS: m/e 254.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09273068B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-20c5ec6bafca4fb0a9ce6892d8c2c734
Quellennotizuspto-grants-2016_03