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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442575Generated: October 28, 2026

Pyridine → HCID 58610107, compound

https://huagongshe.com/reaction/1442575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Mercaptobenzoic AcidHCID 5443—
Reactant2-Methoxybenzoyl chlorideHCID 88969—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58610107HCID 5861010780.2%

Reaction Steps

Thiosalicylic acid (1.38 g, 9.0 mmol) was suspended in tetrahydrofuran (10 ml). While stirring under ice cooling, pyridine (1.77 g, 22 mmol) and then a tetrahydrofuran solution (5 ml) of 2-methoxybenzoyl chloride (1.68 g, 9.9 mmol) were dropwise added to the suspension. After the reaction mixture was stirred for 15 hours, the mixture was diluted with water and 6N hydrochloric acid was added thereto to make its liquid property acidic. The mixture was extracted (50 ml×2) with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was removed by distillation. The residue was recrystallized from tetrahydrofuran-isopropyl ether to give the title compound (2.08 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659267B2
Source datasetuspto-grants-2010_02
ORD IDord-20c50053f8b147cda75d0c118471d1df
Source noteuspto-grants-2010_02