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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231734Generated: October 25, 2026

Acetic Acid → 2-(3'-Chloromethylphenyl)-4-methylthio-6-phenylpyridine

https://huagongshe.com/reaction/231734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium HydroxideHCID 14798—
Reactant1-(3-Chlorophenyl)ethanoneHCID 14933—
Reactant3,3-Bis(methylsulfanyl)-1-phenylprop-2-en-1-oneHCID 280923—
ReactantAmmonium AcetateHCID 517165—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product2-(3'-Chloromethylphenyl)-4-methylthio-6-phenylpyridineHCID 20031588—

Reaction Steps

To 20 ml of tetrahydrofuran solution containing 0.69 g of m-chloroacetophenone was added 1.1 g of potassium t-butoxide at room temperature, followed by stirring for 30 minutes. Further, 1 g of 3,3-bis-(methylthio)-1-phenyl-2-propen-1-one was added, followed by stirring for 1 hour. Subsequently, 20 ml of acetic acid and 3 g of ammonium acetate were added, and reaction was carried out for 3 hours under reflux, while distilling away tetrahydrofuran. The reaction liquid was neutralized with an aqueous solution of sodium hydroxide, and the neutralized solution was extracted twice with 50 ml portions of ethyl acetate. The extract was dried with anhydrous magnesium sulfate. Ethyl acetate was distilled away under reduced pressure and the residues were recrystallized from isopropanol to give 1.1 g of 2-(3'-chloromethylphenyl)-4-methylthio-6-phenylpyridine. (m.p. 56.8° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04849011
Source datasetuspto-grants-1989_07
ORD IDord-b0180c25d7db438096a5fdf4eb33bfd0
Source noteuspto-grants-1989_07