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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637117Generated: November 1, 2026

Pyridine → 2-Methylsulfinyl-5-(1H-tetrazol-1-yl)benzoic Acid

https://huagongshe.com/reaction/637117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
Reactant2-Methylthio-5-(1H-tetrazol-1-yl)benzoic AcidHCID 18464518—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Methylsulfinyl-5-(1H-tetrazol-1-yl)benzoic AcidHCID 18464505—

Reaction Steps

Combine 2-methylthio-5-(1H-tetrazol-1-yl)benzoic acid (0.50 g, 2.0 mmol), pyridine (20 mL) and water (20 mL). Cool in an ice bath. Add phenyltrimethylammonium tribromide (0.75 g, 2 mmol) and tetrahydrofuran (20 mL). Warm to ambient temperature. After 1 hour, add a solution of sodium bisulfite (1 g) in water (1 mL). Extract the reaction mixture with ethyl acetate and then dichloromethane. Combine the organic layers, dry over MgSO4, filter, and evaporate in vacuo to give a residue. the title compound. Chromatograph the residue on silica gel eluting sequentially with ethyl acetate and then 10% methanol/ethyl acetate to give methyl 2-methylsulfinyl-5-(1H-tetrazol-1-yl)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194406B1
Source datasetuspto-grants-2001_02
ORD IDord-2b5e3cada9e041b4a625bad2d9d3e476
Source noteuspto-grants-2001_02