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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 561997Erstellt: 24. Oktober 2026

Acetaldehyde → 1-(2,6-Difluoro-4-iodophenyl)ethanol

https://huagongshe.com/de/reaction/561997

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetaldehydeHCID 177—
Edukt1,3-Difluoro-5-iodobenzeneHCID 2778221—
Edukt1,2,2,3-TetramethylpiperidineHCID 18761772—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(2,6-Difluoro-4-iodophenyl)ethanolHCID 6700129947,4%

Reaktionsschritte

To a solution of 2.5 M n-butyl lithium in hexanes (2 mL, 5.0 mmol) and tetrahydrofuran (20 mL) at −78° C. under an atmosphere of nitrogen was added dropwise tetramethylpiperidine (0.85 mL, 5.0 mmol). The resulting light yellow solution was stirred for approximately 15 minutes, then 1,3-difluoro-5-iodo-benzene (1 g, 4.17 mmol) was added dropwise. This solution was stirred at −78° C. for 1 hour, followed by the addition of acetaldehyde (0.70 mL, 12.5 mmol) via syringe. The reaction mixture was stirred at −78° C. for 10 minutes then allowed to warm to room temperature. TLC indicated the reaction to be complete. The reaction was quenched with saturated aqueous ammonium chloride solution (2 mL), diluted with water (50 mL) and extracted with ethyl acetate (2×30 mL). The combined organic layers were dried over sodium sulfate and concentrated in vacuo. The crude product was purified by chromatography over silica gel gradient eluted with 0 to 25% v/v ethyl acetate/hexanes to give 1-(2,6-difluoro-4-iodo-phenyl)-ethanol (561 mg, 47%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063085B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-4732835dd49a442cbe2e7f06b3806d3e
Quellennotizuspto-grants-2011_11