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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 965466Erstellt: 25. Oktober 2026

tert-Butanol → tert-Butyl Crotonate

https://huagongshe.com/reaction/965466

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-ButanolHCID 6386—
EduktTetrahydrofuranHCID 8028—
EduktCrotyl chlorideHCID 11589—
EduktButyllithiumHCID 178418339—
Produkttert-Butyl CrotonateHCID 5463127—

Reaktionsschritte

A solution of t-BuOH (0.50 mol, 37.1 g, 47.8 mls) in THF (500 mls) is cooled to 5° C.; then over a 30 minute period n-BuLi (0.56 mol., 350 ml, 1.6M) is added to the solution. The resulting mixture is stirred for 40 minutes at room temperature. Crotyl chloride (0.50 mol., 52.3 g, 47.9 mls) in THF (250 mls) is added to the reaction mixture at room temperature over a 15 minute period. The resulting mixture is heated under reflux for 50 minutes. The reaction mixture is cooled to 0° C. and ice-water (800 mls) is added. The layers are separated and the aqueous layer is extracted with Et2O (3×600 mls). The organic phases are combined, dried over Na2SO4, filtered and concentrated by rotary evaporation to give a red oil. Distillation (55° C., 22 mm) yields t-butyl crotonate: 1H NMR (300 MHz, CDCl3) δ 1.46 (s, 9H), 1.83 (dd, J is 6.9, 1.7 Hz, 3H), 5.74 (dq, J is 15.5, 1.7 Hz, 1H), 6.85 (dq, J is 15.5, 6.9 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05773610
Quelldatensatzuspto-grants-1998_06
ORD IDord-57b2c21d8cc24027b090ff7d50c98886
Quellennotizuspto-grants-1998_06