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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1911818Erstellt: 27. Oktober 2026

Chlorotrimethylsilane → 2,6-Dichloro-4-trifluoromethyl-3-trimethylsilanylpyridine

https://huagongshe.com/reaction/1911818

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorotrimethylsilaneHCID 6397—
EduktDiisopropylamineHCID 7912—
EduktHexaneHCID 8058—
Edukt2,6-Dichloro-4-(trifluoromethyl)pyridineHCID 520968—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2,6-Dichloro-4-trifluoromethyl-3-trimethylsilanylpyridineHCID 8671900295%

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

A dry 100 mL 3 neck rb flask was charged with diisopropylamine (2.15 mL, 15.3 mmol) and 40 mL of anhydrous THF. Reaction mixture was cooled at −20° C. under N2. A 2.5 M solution of n-BuLi in Hexane (5.90 mL, 14.8 mmol) was added dropwise via a syringe. The resulting reaction mixture was then cooled at −78° C. A solution of 2,6-dichloro-4-trifluoromethylpyridine (3.0 g, 14 mmol) in 5 mL of anhydrous THF was added slowly via an addition funnel to give a pale yellow solution. Reaction mixture stirred at −78° C. for 2 h. After which time, a solution of TMSCl (2.0 mL, 15.8 mmol) in 5 mL of THF was added dropwise via an addition funnel. The resulting reaction mixture was allowed to slowly warm up to room temperature and stirred over night. Reaction mixture was added to 150 mL of Et2O, washed with dilute HCl, then washed with aq. NaHCO3, dried over MgSO4, filtered and concentrated to give 3.80 g (95%) of 2,6-dichloro-4-trifluoromethyl-3-trimethylsilanylpyridine (Compound 8) as a brown oil:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08604199B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-c635147bd0c941febf6e6a613390cb22
Quellennotizuspto-grants-2013_12