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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210135Generated: October 30, 2026

Methanol → 3-(Phthalimidomethylthio)pyridine

https://huagongshe.com/reaction/2210135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantN,N-dimethyl-1-(pyridin-3-ylsulfanyl)formamideHCID 299059—
SolventEthanolHCID 702—
Product3-(Phthalimidomethylthio)pyridineHCID 1907913880.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 1.00 g (5.49 mmol) of 3-(dimethylaminocarbonylthio)pyridine in 50 ml of methanol, 5.49 ml (5.49 mmol) of a 1N aqueous solution of sodium hydroxide was added. The mixture was heated at 60° C. for 1 hour with stirring. After cooling, the solvent was distilled off. The residue was dissolved in ethanol and dried. The solvent was distilled off. The residue thus obtained and 1.58 g of (6.59 mmol) of (N-bromomethyl)phthalimide were suspended in 50 ml of ethanol, and 0.92 ml (6.59 mmol) of triethylamine was added. The mixture was stirred at room temperature for 4 hours. The solvent was distilled off, and the residue was dissolved in chloroform, washed with water and dried. Then the solvent was distilled off. The residue was purified by column chromatography (eluent: hexane/ethyl acetate=1:1) to obtain powder. The powder thus obtained was washed with ether and dried to obtain 1.20 g of the desired compound (yield: 80.9% colorless powder)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457106
Source datasetuspto-grants-1995_10
ORD IDord-9a8d20fd0f594c93b42142f4df2fa298
Source noteuspto-grants-1995_10