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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35546Generated: October 28, 2026

4-Methoxy-alpha-toluenethiol → Methyl 3-[[(4-methoxyphenyl)methyl]thio]-2-pyridinecarboxylate

https://huagongshe.com/reaction/35546

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-alpha-toluenethiolHCID 80407—
ReactantSodium methanolate methanolHCID 23694274—
Reactantmethyl 3-(N,N-dimethylaminocarbamoylthio)pyridine-2-carboxylateHCID 86742402—
SolventMethanolHCID 887—
ProductMethyl 3-[[(4-methoxyphenyl)methyl]thio]-2-pyridinecarboxylateHCID 1427762262.2%

Reaction Steps

A solution of 1.20 g (5 mmol) of methyl 3-(N,N-dimethylaminocarbamoylthio)pyridine-2-carboxylate in 5 mL of methanol and 1.5 mL (6 mmol) of 4.1M sodium methoxide methanol was stirred at room temperature for 10 minutes. Then the solvent was concentrated and the residue was dissolved in 5 mL of N,N-dimethylformamide and 5 mL of tetrahydrofuran. 0.936 g (6 mmol) of p-methoxybenzylmercaptan was added and the solution was stirred at room temperature for 18 hours. The solution was partitioned between ether and water and the aqueous layer was extracted with two portions of ether. The combined extracts were washed with brine, dried and concentrated. Recrystallization from methanol afforded 0.90 g (62%) of pale tan needles, m.p. 99°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767766
Source datasetuspto-grants-1988_08
ORD IDord-08c753c85ed74497a3034fb16b17f6e1
Source noteuspto-grants-1988_08