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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1200004Erstellt: 26. Oktober 2026

Methyl iodide → Methyl 2-(3-methoxybenzylthio)nicotinate

https://huagongshe.com/reaction/1200004

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
Edukt2-(3-Methoxybenzylthio)nicotinic acidHCID 859340—
LösungsmittelAcetonitrileHCID 6342—
ProduktMethyl 2-(3-methoxybenzylthio)nicotinateHCID 1427764592%

Reaktionsschritte

A suspension of 7.15 g (0.026 mole) of 2-(3-methoxybenzylthio)nicotinic acid in 75 ml of dry acetonitrile was treated with 3.95 g (0.026 mole) of 1,8-diazabicyclo[5,4,0]-under-7-ene (DBU). A solution formed and 4.26 g (0.030 mole) of methyl iodide was added over one minute. After keeping the reaction mixture at room temperature for 24 hours, the solution was evaporated in vacuo. The residue was partitioned between 100 ml of ether and 50 ml of water. The ether layer was washed with 50 ml of H2O, dried, and evaporated to a small volume. The addition of hexane with cooling yielded 6.9 g (92% of theory) of methyl 2-(3-methoxybenzylthio)nicotinate; m.p. 69°-70° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04904672
Quelldatensatzuspto-grants-1990_02
ORD IDord-4c7eadf0d4634414b90c69607db25147
Quellennotizuspto-grants-1990_02