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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649134Generated: November 1, 2026

Sodium Hydroxide → 2-{[(2-Methoxyphenyl)sulfanyl]methyl}pyridine--hydrogen chloride (1/1)

https://huagongshe.com/reaction/1649134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPicolyl chloride hydrochlorideHCID 23392—
ReactantThioguaiacolHCID 23642—
SolventEthanolHCID 702—
Product2-{[(2-Methoxyphenyl)sulfanyl]methyl}pyridine--hydrogen chloride (1/1)HCID 1295329243%

Reaction Steps

2-Methoxybenzenethiol (5 g) was added to a solution of sodium hydroxide (2.85 g) in ethanol (50 ml) and the resulting mixture was treated with 2-picolyl chloride, hydrochloride (5.7 g) in ethanol (25 ml) at 0° C. After 16 hours at ambient temperature the mixture was filtered through kieselghur and evaporated. The residue was converted into the hydrochloride in ether with ethereal HCl solution and this was recrystallised from propan-2-ol/acetone to give 2-(((2-methoxyphenyl)thio)methyl)pyridine, hydrochloride (4.0 g) mp 141°-3° C. (Found: C,58.5; H,5.4; N,4.9 C13H13NOS.HCl requires C,58.3; H,5.3; N,5.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04415579
Source datasetuspto-grants-1983_11
ORD IDord-5993ef00736e433dad18df4a966582cd
Source noteuspto-grants-1983_11