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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 53273Erstellt: 23. Oktober 2026

Methyl iodide → Methyl 4-ethenylbenzoate

https://huagongshe.com/de/reaction/53273

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktEthyl AcetateHCID 8857—
Edukt4-Vinylbenzoic acidHCID 14098—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
LösungsmittelAcetonitrileHCID 6342—
ProduktMethyl 4-ethenylbenzoateHCID 583124—

Reaktionsschritte

To a solution of 4-vinylbenzoic acid (Aldrich, 2.18 g, 14.7 mmol) in anhydrous acetonitrile (14.0 mL) was added 1.8-diazabicyclo [5.4.0]undec-7-ene (Aldrich, 2.46 g, 16.2 mmol) and iodomethane (Aldrich, 3.13 g, 2.1 mmol) at 0° C. The reaction mixture was then warmed to room temperature and allowed to stir for 3 h. Ethyl acetate (100 mL) was added to the mixture and the solution was washed with brine (50 mL). The organic phase was then separated and concentrated in vacuo. The residue was chromatographed on silica gel (eluted with 5% ethyl acetate in hexane) to give 1.05 g (Y: 44%) of the title product; 1H-NMR (CDCl3): δ8.00 (d, J=8.4 Hz, 2H), 7.47 (d, J=8.4 Hz, 2H), 6.76 (m, 1H), 5.87 (d, J=17.6 Hz, 1H), 5.38 (d, J=11.0 Hz, 1H), 3.91 (s, 3H); MS (DCI) m/e: 163 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05618839
Quelldatensatzuspto-grants-1997_04
ORD IDord-0b775bc4eb8d41efbf5bcc45d9cdf8fd
Quellennotizuspto-grants-1997_04