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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 221917Erstellt: 25. Oktober 2026

Dimethylformamide → 5-Bromo-2-fluoro-4-(hydroxymethyl)benzaldehyde

https://huagongshe.com/reaction/221917

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktAmmonium ChlorideHCID 25517—
Edukt2-Bromo-5-fluorobenzyl alcoholHCID 2773349—
Edukt1,2,2,3-TetramethylpiperidineHCID 18761772—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Bromo-2-fluoro-4-(hydroxymethyl)benzaldehydeHCID 59278930106,7%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Tetramethylpiperidine (0.68 g, 4.87 mmol) was dissolved in tetrahydrofuran (4.5 mL). To the resultant solution was added n-butyllithium (1.0 M n-hexane solution, 4.88 mL) at 0° C., and the solution was then stirred for 15 minutes. The solution was cooled to −78° C., and a solution of (2-bromo-5-fluorophenyl)-methanol (0.50 g, 2.43 mmol) in tetrahydrofuran (2.5 mL) was added dropwise. The temperature of the solution was raised over 2 hours to −40° C. The solution was again cooled to −78° C., and N,N-dimethylformamide (0.47 mL, 6.07 mmol) was added thereto. The temperature of the solution was raised to room temperature, and the solution was then stirred for 30 minutes. Saturated aqueous ammonium chloride was added, and the resultant mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and then concentrated under reduced pressure, to thereby obtain the titled compound (604.3 mg, quantitative).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08207134B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-f40641d84fb74929ad904fe03f5c0e41
Quellennotizuspto-grants-2012_06