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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084731Generated: October 26, 2026

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

https://huagongshe.com/reaction/1084731

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 numberUS05006532
Source datasetuspto-grants-1991_04
ORD IDord-372a19b4fff44ccfaab74968401fc9bc
Source noteuspto-grants-1991_04