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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279867Erstellt: 25. Oktober 2026

2-Bromostyrene → Benzaldehyde, 2-ethenyl-

https://huagongshe.com/reaction/279867

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-BromostyreneHCID 16264—
Edukt1-PiperidinecarboxaldehydeHCID 17429—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
ProduktBenzaldehyde, 2-ethenyl-HCID 39391—

Reaktionsbedingungen

Temperatur-65 °C

Reaktionsschritte

To a solution of 2-bromostyrene (115 mmol) in dry tetrahydrofuran (200 ml) at -65° C. under nitrogen was added dropwise n-butyllithium (115 mmol) in hexane. The reaction mixture was stirred at -65° C. for an additional hour and a solution of N-formylpiperidine (125 mmol) in tetrahydrofuran (50 ml) was added dropwise. The reaction mixture was allowed to warm to ambient temperature overnight. The reaction mixture was cooled to 0° C. and then quenched with saturated ammonium chloride (50 ml). The reaction mixture was extracted with diethyl ether (2×50 ml) and the combined organic phases were washed with 3N hydrochloric acid (2×50 ml), saturated aqueous sodium bicarbonate (50 ml), and brine, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo to yield the Compound 2a which was directly used in the next reaction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04587253
Quelldatensatzuspto-grants-1986_05
ORD IDord-c1c226ff46244816b56974bf4ddc5953
Quellennotizuspto-grants-1986_05