Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 471171Erstellt: 26. Oktober 2026

Dimethylformamide → 3-(2-(tert-Butyldimethylsilyloxy)ethyl)-2-fluorobenzaldehyde

https://huagongshe.com/reaction/471171

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPentamethyldiethylenetriamineHCID 18196—
Edukttert-Butyl(2-fluorophenethoxy)dimethylsilaneHCID 57988979—
EduktCID 53628100HCID 178418400—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(2-(tert-Butyldimethylsilyloxy)ethyl)-2-fluorobenzaldehydeHCID 57989164—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

tert-Butyl(2-fluorophenethoxy)dimethylsilane (example 78, step a) (5.00 g) was added over 5 minutes to a stirred solution of sec-butyllithium (1.4 molar solution in cyclohexane, 14.0 mL) and N1-(2-(dimethylamino)ethyl)-N1,N2,N2-trimethylethane-1,2-diamine (4.10 mL) in THF (25 mL) cooled to −78° C. After 2 h, N,N-dimethylformamide (10.06 g) was added, the reaction mixture was stirred at −78° C. for 1 h, and then the cooling bath was removed. After a further 0.5 h, the reaction was quenched with water. Ethyl acetate (300 mL) was added and the reaction mixture washed with water (3×150 mL), 2M HCl (2×50 mL), water (2×50 mL), brine then dried over sodium sulphate, filtered and evaporated in vacuo to give the subtitled compound as an oil. Yield 5.3 g.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08629271B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-e3b7cb78208e441492fc35e6b4e5c1aa
Quellennotizuspto-grants-2014_01