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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1200004Generated: October 25, 2026

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

https://huagongshe.com/reaction/1200004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-(3-Methoxybenzylthio)nicotinic acidHCID 859340—
SolventAcetonitrileHCID 6342—
ProductMethyl 2-(3-methoxybenzylthio)nicotinateHCID 1427764592%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04904672
Source datasetuspto-grants-1990_02
ORD IDord-4c7eadf0d4634414b90c69607db25147
Source noteuspto-grants-1990_02