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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349259Erstellt: 25. Oktober 2026

Dimethylformamide → HCID 11332876, Verbindung

https://huagongshe.com/reaction/349259

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt((1,1-Dimethyl-2-propynyl)oxy)trimethylsilaneHCID 87344—
EduktMonobasic potassium phosphateHCID 516951—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelCyclohexaneHCID 8078—
ProduktHCID 11332876HCID 11332876—

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

Dissolve 3-methyl-3-trimethylsilyloxy-1-butyne (8.35 g, 53.4 mmol) in THF (200 mL) and cool to 40° C. Add n-butyllithium (26.7 mL of a 2.0 M solution in cyclohexane, 53.4 mmol, 1 eq.) dropwise over a 5 minute period. Stir for 10 min., then add dry DMF (8.27 mL, 7.81 g, 107 mmol, 2 eq.) in one portion. After 30 min., pour into a cooled (0° C.), vigorously stirred mixture of 10% KH2PO4 (290 mL, 213 mmol) and ether (300 mL). Separate the layers and wash the organic layer with water (2×200 mL). Dry (MgSO4), filter, and concentrate to give 9.4 g (94% crude) of a light oil. Use without further purification. TLC: Rf=0.40 (20:1 hexanes/EtOAc); 1H NMR (CDCl3, 300 MHz) δ 9.03 (s, 1H), 1.35 (s, 6H), 0.02 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07179804B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-a124a82e2f8a48a6ae79ee58cffde1a1
Quellennotizuspto-grants-2007_02