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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389801Generated: October 25, 2026

2-Mercaptoethanol → 2-[(2-Pyridin-4-ylethyl)thio]ethanol

https://huagongshe.com/reaction/1389801

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MercaptoethanolHCID 1567—
Reactant4-VinylpyridineHCID 7502—
ReactantSodium MethoxideHCID 10942334—
SolventEthanolHCID 702—
Product2-[(2-Pyridin-4-ylethyl)thio]ethanolHCID 2058406—

Reaction Steps

Under a nitrogen atmosphere, sodium methoxide (1.62 g., 0.03 mole) was dissolved in 36 ml. of stirring absolute ethanol and the solution cooled in an ice bath. 2-Mercaptoethanol (2.34 g., 0.03 mole) in 6 ml. of absolute ethanol was added over approximately 5 minutes. Finally, 4-vinylpyridine (3.22 g., 0.03 mole) in approximately 20 ml. of absolute ethanol was added over 15 minutes. The reaction mixture was allowed to warm to room temperature and stirred for 23 hours. The reaction mixture was concentrated to a thick oil (7.28 g.). The oil was diluted with a small amount of chloroform (a strong exotherm occurred, leading to refluxing of the chloroform) and chromatographed on silica gel, with large volumes of chloroform and finally chloroform/1% methanol as eluant. Product containing fractions (from the latter eluant) were combined and evaporated to yield the free base of 4-[2-(2-hydroxyethylthio)ethyl]pyridine [2.49 g.; oil; m/e calcd.: 183, found: 183; ir (film): 3.10, 3.45, 3.52, 6.23, 7.07, 9.40, 9.57, 9.98 and 12.44μ; pnmr/CDCl3 /TMS/δ: 8.53 (m, 2H), 7.17 (m, 2H), 3.77 (t, 2H), 3.57 (s, 1H, exchanges with D2O), 2.85 (m, 4H) and 2.73 ppm (t, 2H)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04246263
Source datasetuspto-grants-1981_01
ORD IDord-13b70061753f4a89be0102c5618fb7c9
Source noteuspto-grants-1981_01